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58-14-0

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58-14-0 Usage

Pharmacology and mechanism of action

Pyrimethamine is a diaminopyrimidine which is structurally related to trimethoprim. It is effective against erythrocytic stage of Plasmodium (P) falciparum and less so against P. vivax, P. ovale and P. malariae. Pyrimethamine also inhibits the sporogony in the mosquito, resulting in a decrease of transmission of the infection within the community [1]. The mechanism of action of pyrimethamine is related to its inhibition of dihydrofolic reductase necessary for the folic acid synthesis in the parasite. Pyrimethamine acts slowly and is not recommended as monotherapy for acute malaria attacks. Resistance to pyrimethamine developed soon when the drug was used on a large scale as monoprophylaxis [1]. In resistant strains, the enzyme dihydrofolic reductase binds to pyrimethamine several hundred times less than in sensitive strains [2]. This high grade resistance is probably a onestep mutation and cannot be overcome by increasing the dose. However, when combined with long-acting sulphonomides (sulphadoxine), the effect of pyrimethamine is potentiated and the risk of developing resistant strains is far less.

Preparations

Pyrimethamine combined with sulphadoxine. ? ? Fansidar? (Roche). Tablets (pyrimethamine 25 mg plus sulphadoxine 500 mg). Solution for intramuscular injection (pyrimethamine 10 mg/ml and sulphadoxine 200 mg/ml).

Antiprotozoal veterinary drug

Pyrimethamine is a widely used broad-spectrum antiprotozoal veterinary medicine. In addition to this, pyrimethamine can also be applied to the breeding of the aquatic product and is also capable of enhancing the disease resistance capability of aquaculture fish. However, pyrimethamine has significant side effects with being used in excess amount being able to cause damage to the reproductive system of livestock and poultry, and is also difficult for recovery. Pyrimethamine has inhibitory effect on the primary exo-erythrocytic stage of Plasmodium falciparum and vivax malaria, and is a good preventive medicine. Although it has no significant effects on the malaria gametocyte but when the drug-containing blood enters into the mosquito body, it can affect the development of gametocytes inside mosquitoes, thus being able to interrupt the transmission. The mechanism of action is to inhibit the dihydrofolate reductase and affect the utilization of folate, causing reduction of the nucleic acid synthesis and inhibiting the malaria parasite reproduction. Meanwhile pyrimethamine and chloroquine, through lowering the level of oxidative stress and apoptosis, can exert protective effect on the placental pathology after the infection of malaria and can also reduce the proportion of infected red cells in the blood, therefore being able to achieving a excellent therapeutic effect on malaria. It also has enrichment effect in aquatic body. Upon going beyond a certain range, it can cause hemolytic anemia after being eaten and even has direct toxicity on the central nervous system. This product is mainly used for the prevention of malaria and can also be used for the treatment of toxoplasmosis. It has inhibitory effects on the primary exo-erythrocytic stage of some kinds of Plasmodium falciparum and vivax malaria and is a good preventive medicine. Owing to its slow excretion rate, it has a long-lasting effect with the preventive effect of one-time medication being able to be maintained for more than 1 week. Although this product has no significant effects on the malaria gametocyte but when the drug-containing blood is inhaled into the mosquito body, it can affect the development of gametocytes inside mosquitoes, thus being able to interrupt the transmission. Because of its effect on inhibiting the exo-erythrocytic stage of Plasmodium, it is usually used in combination with primaquine for the prevention of recurrence. This product appears as white crystalline powder; it is odorless and tasteless. It is insoluble in water, slightly soluble in ethanol, chloroform and acetone and soluble in dilute acid. It has a melting point of 232~235 ℃. Figure 1 is a structural formula of pyrimethamine

Role and purpose

This product can inhibit dihydrofolate reductase, causing failure of the conversion from dihydrofolate into tetrahydrofolate, resulting in decreased synthesis of nucleic acid, so that the parasite propagation is inhibited. It is mainly used for the prevention of malaria, it can also be combined with primaquine to prevent relapse of malaria.

Pharmacokinetics

After oral administration, gastrointestinal absorption is complete but very slow with the blood concentration reaching peak after four hours. Plasma protein has a binding rate of 80%. It is mainly distributed in tissues such as liver, lung, kidney and other tissues as well as in milk. The half-life is about 90 hours with only 10% to 20% of the prototype drug being excreted through the urine at 5 to 7 days after administration. The effective concentration of the blood can be maintained for two weeks. Therefore, single-time medication can has its preventive effect be maintained for more than 1 week.

Side effects

Different sources of media describe the Side effects of 58-14-0 differently. You can refer to the following data:
1. 1. Upon administration of high dose can cause acute poisoning symptoms such as fatigue, nausea, vomiting, abdominal pain, fever, cyanosis, jaundice, splenomegaly, etc. Upon this condition, drug administration should be promptly discontinued and the patients should be subject to gastric lavage, rehydration and symptomatic treatment. Because of the sweet taste of this product, it is more prone for children to be subject to mistakenly administration and poisoning, special attention should be paid. 2. Long-term administration can interfere with the in vivo utilization of folic acid, producing megaloblastic anemia. Therefore, the patients should be subject to regularly monitoring of blood. If the above issue happens, we should treat with leucovorin.
2. Relatively few side effects are associated with the usual antimalarial dosages. However, signs of toxicity are evident at higher dosages, particularly those used in the management of toxoplasmosis. Many of these reactions reflect the interference of pyrimethamine with host folic acid metabolism, especially that occurring in rapidly dividing cells. Toxic symptoms include anorexia, vomiting, anemia, leukopenia, thrombocytopenia, and atrophic glossitis. CNS stimulation, including convulsions, may follow an acute overdose.The side effects associated with the pyrimethamine–sulfadoxine combination include those associated with the sulfonamide and pyrimethamine alone. In addition, there is evidence of a greater incidence of allergic reactions, particularly toxic epidermal necrolysis and Stevens-Johnson syndrome, with the combination. This carries an estimated mortality of 1:11,000 to 1:25,000 when used as a chemoprophylactic.

Precautions

1. Lactating women and patients of renal dysfunction should take with caution. Pregnant women in early phase should be disabled. Children less than 1 year of age should not use. 2. This product has slightly fragrance without bitter taste and should be protected from the reach of children whose mistaken administration can lead to poisoning, convulsions (Children under age 6 who takes 50~100mg can get poisoning and die). Barbiturates can confront its role in the central excitability. 3. This product, after single-time overdose of long-term continuous administration can cause bone marrow suppression and gastrointestinal function inhibition, resulting in megaloblastic anemia and leukopenia with timely withdrawal leading to self-healing. Giving formylation CF may alleviate the bone marrow function. 4. Adults, after single dose administration of 150~200mg have the risk of poisoning. It often occurs of nausea, vomiting, headache, dizziness and other symptoms within 1 to 5 hours with convulsions and coma occurring in severe cases. Children under 6 years of age can die upon administration at draught of 50~100mg and get poisoning and die, it should be given attention. First aid measures: apply gastric lavage, vomiting; drink a lot of sugar or 10% carrot juice. The patients can further subject to administration of the glucose infusion and diuretics. Patients of spasms and convulsions should be subject to infusion of thiopental. 5. Patients of renal damage, unconsciousness, 6-GPD deficiency and giant cell anemia should take with caution. This information is edited by Xiongfeng Dai from lookchem.

Medicine interactions

Being used in combination with dihydrofolate synthetase inhibitors (such as sulfadoxine or dapsone) can double block the folate metabolism of malaria parasite and enhance its performance, delay or prevent the emergence of drug-resistant strains of insects. It can’t be used in combination with other kinds of dihydrofolate reductase inhibitor because it can enhance the toxicity.

Dosage

Prophylaxis: start administration at 1 to 2 weeks before entering into the affected area. It is generally recommended to keep administration to until 6 to 8 weeks after leaving the affected areas once per week and 25 mg per time. Children take once per week with 0.9 mg/kg per time with the highest dose limited for adults. For Plasmodium falciparum caused chloroquine-resistant strains: take 50 mg daily with 2 times. For children, take 0.3 mg/kg at 3 times per day with the course of three days. Toxoplasmosis: Daily 50~100 mg, administrate at draught at a dose of 25 mg after 1 to 3 days with a course of 4 to 6 weeks. For children, take 1 mg/kg with 2 times. After 1-3 days, change to 0.5 mg/kg daily at 2 times with a course of 4 to 6 weeks.

References

1. Black RH, Canfield CJ, Clyde DF, Peters W, Wernsdorfer WH (1986). Chemotherapy of Malaria, 2nd edn, edited by L.J.Bruce-Chwatt. (Geneva: World Health Organization), pp. 77–80. 2. The biology of malaria parasites. Technical Report Series no 743 (1987). (Geneva: World Health Organization). 3. Friman G, Nystr?m-Rosander C, Jonsell G, Bj?rkman A, Svendsrup B (1985). Agranulocytosis associated with malaria prophylaxis with Maloprim. BMJ, 286, 1244–1245. 4. Pyrimethamine. Therapeutic Drugs, edited by Sir Colin Dollery (1991), (London: Churchill Livingstone), pp. P314–P317.

Chemical Properties

White Solid

Uses

Different sources of media describe the Uses of 58-14-0 differently. You can refer to the following data:
1. For the treatment of toxoplasmosis and acute malaria; For the prevention of malaria in areas non-resistant to pyrimethamine. Pyrimethamine is a dihydrofolate reductase inhibitor, like the biguanides, and is structurally related to trimethoprim. It is seldom used alone. Pyrimethamine in fixed combinations with dapsone or sulfadoxine is used for treatment and prophylaxis of chloroquine-resistant falciparum malaria. The synergistic activities of pyrimethamine and sulfonamides are similar to those of trimethoprim/sulfonamide combinations. Resistant strains of Plasmodium falciparum have appeared world wide. Prophylaxis against falciparum malaria with pyrimethamine alone is therefore not recommended. Most strains of Plasmodium vivax have remained sensitive. Pyrimethamine is also used in combination with a sulfonamide for the treatment of Toxoplasmosis. It is slowly absorbed from the gastrointestinal tract with peak plasma levels 4–6 hours after dosing. Pyrimethamine is bound to plasma proteins and is extensively metabolized before excretion. Its elimination half-life is 3–5 days.
2. This powerful inhibitor of dihydrofolate reductase is used for preventing and treating malaria caused by plasmodia P. vivax, P. malariae, P. ovale, including P. falciparum. Pyrimethamine, an antagonist of folic acid, exhibits antimicrobial action against causative agents of malaria and simultaneously possesses sporontocide action. It is also effective with respect to the causative agent of toxoplasmosis. It is used for preventing malaria and treating toxoplasmosis. It can only be used for preventative measures; however, because resistance develops quickly and because of the fact that the maximal effect is achieved by using it in combination with sulfadoxine, a combined drug which is prescribed under the name fansidar, which contains a pyrimethamine–sulfadoxine ratio of 1:20. A combination of pyrimethamine, sulfonamide, and quinine is the drug of choice for acute attacks of malaria and its chloroquine-resistant forms. Pyrimethamine in combination with sulfadiazine or trisulfapyrimidine is the drug of choice for toxoplasmosis. A synonym of this combined drug is daraprim.
3. Dihydrofolate reductase inhibitor; generally used in combination with other antimicrobial agents. Antiprotozoal (Toxoplasma); antimalarial

Indications

Pyrimethamine (Daraprim) is the best of a number of 2,4- diaminopyrimidines that were synthesized as potential antimalarial and antibacterial compounds. Trimethoprim (Proloprim) is a closely related compound. Pyrimethamine is well absorbed after oral administration, with peak plasma levels occurring within 3 to 7 hours. An initial loading dose to saturate nonspecific binding sites is not required, as it is with chloroquine. However, the drug binds to tissues, and therefore, its rate of renal excretion is slow. Pyrimethamine has a half-life of about 4 days. Although the drug does undergo some metabolic alterations, the metabolites formed have not been totally identified.

Definition

ChEBI: An aminopyrimidine that is pyrimidine-2,4-diamine which is substituted at position 5 by a p-chlorophenyl group and at position 6 by an ethyl group. It is a folic acid antagonist used as an antimalarial or with a sulfonamide to treat toxoplasmo is.

Brand name

Daraprim (GlaxoSmithKline).

General Description

Odorless white crystalline powder. Tasteless. An antimalarial drug.

Air & Water Reactions

Pyrimethamine is a diaminopyrimidine which is structurally related to trimethoprim. It is effective against erythrocytic stage of Plasmodium (P) falciparum and less so against P. vivax, P. ovale and P. malariae. Pyrimethamine also inhibits the sporogony in the mosquito, resulting in a decrease of transmission of the infection within the community[1]. The mechanism of action of pyrimethamine is related to its inhibition of dihydrofolic reductase necessary for the folic acid synthesis in the parasite. Pyrimethamine acts slowly and is not recommended as monotherapy for acute malaria attacks. Resistance to pyrimethamine developed soon when the drug was used on a large scale as monoprophylaxis [1]. In resistant strains, the enzyme dihydrofolic reductase binds to pyrimethamine several hundred times less than in sensitive strains [2]. This high grade resistance is probably a onestep mutation and cannot be overcome by increasing the dose. However, when combined with long-acting sulphonomides (sulphadoxine), the effect of pyrimethamine is potentiated and the risk of developing resistant strains is far less.

Reactivity Profile

Pyrimethamine together with sulphadoxine (Fansidar) is used in the treatment of P. falciparum malaria (cf. Sulphadoxine: Indications). Pyrimethamine is also valuable in the treatment of toxoplasmosis.

Fire Hazard

Pyrimethamine in combination with sulphadoxine (Fansidar) can cause severe cutaneous adverse reactions (cf. Sulphadoxine: Side effects). Agranulocytosis occurs quite frequently (1/2000) and fatalities have been reported when pyrimethamine is combined with dapsone [3]. When given alone, life-threatening adverse reactions are very rare and the drug is generally well tolerated. Megaloblastic anaemia may, however, occur during long-term treatment with high doses (i.e. for toxoplasmosis) and can be prevented by folinic acid supplementation [4].

Biological Activity

During long-term treatment with high doses, folinic acid supplement is usually given.

Mechanism of action

The combination of pyrimethamine with a long-acting sulfonamide, sulfadoxine, which blocks dihydrofolate synthesis by blocking incorporation of PABA into the dihydrofolate, is called Fansidar, which produces sequential blockage of tetrahydrofolate synthesis similar to that reported for treatment of bacterial infections. Plasmodium enzymes catalyzing folic acid synthesis differ from those enzymes found in other organisms. A single bifunctional protein present in Plasmodium sp. catalyzes the phosphorylation of 6-hydroxymethyl-7,8-hydropterin (a pyrophosphokinase) and the incorporation of PABA into dihydropteroic acid. A second bifunctional enzyme catalyzes the reduction of dihydropteroic acid and thymidylic acid synthesis. As a result, the drug combination (Fansidar) appears to have improved drug-mediated disruption of folic acid in Plasmodium sp.. This combination has been used with quinine for the treatment and prevention of chloroquine-resistant malaria (Plasmodium falciparum, Plasmodium ovale, Plasmodium vivax, and Plasmodium malaria). The combination therapy (Fansidar) has the added advantage of being inexpensive, which is essential for successful therapy in developing countries. When used on its own, pyrimethamine is a blood schizonticide without effects on the tissue stage of the disease.

Clinical Use

Pyrimethamine has been recommended for prophylactic use against all susceptible strains of plasmodia; however, it should not be used as the sole therapeutic agent for treating acute malarial attacks. As mentioned previously, sulfonamides should always be coadministered with pyrimethamine (or trimethoprim), since the combined antimalarial activity of the two drugs is significantly greater than when either drug is used alone. Also, resistance develops more slowly when they are used in combination. Sulfonamides exert little or no effect on the blood stages of P. vivax, and resistance to the dihydrofolate reductase inhibitors is widespread. In addition to its antimalarial effects, pyrimethamine is indicated (in combination with a sulfonamide) for the treatment of toxoplasmosis.The dosage required is 10 to 20 times higher than that employed in malarial infections.

Safety Profile

Poison by ingestion, subcutaneous, and intraperitoneal routes. Experimental teratogenic and reproductive effects. Questionable carcinogen. Human mutation data reported. When heated to decomposition it emits very toxic fumes of Cland NOx. Used as an antimalarial drug for humans and to treat toxoplasmosis in hogs.

Synthesis

Pyrimethamine, 2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine (33.1.60), is synthesized from 4-chlorobenzycyanide, which upon condensation with methyl ester of propionic acid in the presence of sodium methoxide gives the β-ketonitrile (33.1.58). Reacting this with ethyl orthoformate gives a methoxymethylene derivative (33.1.59), which upon heterocyclization in pyrimidine using guanidine as the binucleophile forms the desired pyrimethamine (33.1.60).

Veterinary Drugs and Treatments

In veterinary medicine, pyrimethamine is used to treat Hepatozoon americanum infections, and toxoplasmosis in small animals (often in combination with sulfonamides). In horses, it is used to treat equine protozoal myeloencephalitis, sometimes called equine toxoplasmosis. In humans, pyrimethamine is used for the treatment of toxoplasmosis and as a prophylactic agent for malaria.

Drug interactions

Potentially hazardous interactions with other drugs Increased antifolate effect with sulphonamides, trimethoprim, methotrexate and pemetrexed. Antiepileptics: anticonvulsant effect of fosphenytoin and phenytoin antagonised, also increased antifolate effect. Antimalarials: avoid concomitant use with artemether/lumefantrine; increased antifolate effect with proguanil.

Metabolism

Pyrimethamine is metabolised in the liver and slowly excreted via the kidney, with up to 30% recovered in the urine as parent compound over a period of several weeks. Several metabolites have also been detected in the urine, although data are lacking on the nature of these metabolites, their route, rate of formation and elimination, and any pharmacological activity, particularly after prolonged daily dosing.

Check Digit Verification of cas no

The CAS Registry Mumber 58-14-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58-14:
(4*5)+(3*8)+(2*1)+(1*4)=50
50 % 10 = 0
So 58-14-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H13ClN4/c1-2-9-10(11(14)17-12(15)16-9)7-3-5-8(13)6-4-7/h3-6H,2H2,1H3,(H4,14,15,16,17)

58-14-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (P2037)  Pyrimethamine  >98.0%(HPLC)(T)

  • 58-14-0

  • 1g

  • 310.00CNY

  • Detail
  • TCI America

  • (P2037)  Pyrimethamine  >98.0%(HPLC)(T)

  • 58-14-0

  • 5g

  • 990.00CNY

  • Detail
  • Sigma-Aldrich

  • (P4200000)  Pyrimethamine  European Pharmacopoeia (EP) Reference Standard

  • 58-14-0

  • P4200000

  • 1,880.19CNY

  • Detail
  • USP

  • (1589007)  Pyrimethamine  United States Pharmacopeia (USP) Reference Standard

  • 58-14-0

  • 1589007-200MG

  • 4,662.45CNY

  • Detail
  • Sigma-Aldrich

  • (46706)  Pyrimethamine  VETRANAL, analytical standard

  • 58-14-0

  • 46706-250MG

  • 479.70CNY

  • Detail

58-14-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name pyrimethamine

1.2 Other means of identification

Product number -
Other names Malacid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58-14-0 SDS

58-14-0Synthetic route

2,4-diamino-5-(3-azido-4-chlorophenyl)-6-ethylpyrimidine
95458-40-5

2,4-diamino-5-(3-azido-4-chlorophenyl)-6-ethylpyrimidine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With hydrazine hydrate for 0.25h; Heating;85%
4-Chlorophenylboronic acid
1679-18-1

4-Chlorophenylboronic acid

2,4-diamino-6-ethyl-5-iodopyrimidine
514854-13-8

2,4-diamino-6-ethyl-5-iodopyrimidine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With dipotassium hydrogenphosphate; Pd(OAc)2(dppf)2 In 1,2-dimethoxyethane for 24h; Suzuki cross-coupling; Heating;76%
5-(4-chlorophenyl)pyrimidine-2,4-diamine
17039-14-4

5-(4-chlorophenyl)pyrimidine-2,4-diamine

Ethyl boronic acid
4433-63-0

Ethyl boronic acid

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Stage #1: 5-(4-chlorophenyl)pyrimidine-2,4-diamine With acetic acid; trifluoroacetic acid In acetonitrile at 20℃; for 0.166667h; Minisci Aromatic Substitution; Green chemistry;
Stage #2: Ethyl boronic acid With oxygen In acetonitrile at 110℃; under 760.051 Torr; for 10h; Minisci Aromatic Substitution; Green chemistry;
74%
C12H12ClN6(1+)*BF4(1-)

C12H12ClN6(1+)*BF4(1-)

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With formamide; triethylamine Ambient temperature;64%
1-(4-chlorophenyl)-1-cyano-2-methoxybut-1-ene

1-(4-chlorophenyl)-1-cyano-2-methoxybut-1-ene

guanidine hydrochloride
50-01-1

guanidine hydrochloride

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With sodium methylate In various solvent(s) for 16h; Heating;50%
α-(4-chlorophenyl)-α-propionylacetonitrile
55474-40-3

α-(4-chlorophenyl)-α-propionylacetonitrile

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With diethyl ether anschliessenden Erwaermen mit Guanidin in Aethanol;
6-ethyl-2-amino-5-(4-chloro-phenyl)-3H-pyrimidine-4-thione
105640-59-3

6-ethyl-2-amino-5-(4-chloro-phenyl)-3H-pyrimidine-4-thione

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With ethanol; ammonia at 180℃;
N-[4-ethyl-6-chloro-5-(4-chloro-phenyl)-pyrimidin-2-yl]-acetamide
100716-90-3

N-[4-ethyl-6-chloro-5-(4-chloro-phenyl)-pyrimidin-2-yl]-acetamide

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With ethanol; ammonia at 155℃;
With ammonia; phenol at 110℃;
2-(4-chloro-phenyl)-3-isobutoxy-pent-2-enenitrile
67466-67-5

2-(4-chloro-phenyl)-3-isobutoxy-pent-2-enenitrile

sodium ethanolate
141-52-6

sodium ethanolate

guanidine nitrate
506-93-4

guanidine nitrate

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With ethanol
3-anilino-2-(4-chloro-phenyl)-pent-2-enenitrile

3-anilino-2-(4-chloro-phenyl)-pent-2-enenitrile

Triethyl orthoacetate
78-39-7

Triethyl orthoacetate

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
anschliessenden Erhitzen mit Guanidin in Aethanol auf 130grad/2 Torr;
Diacetamidopyrimethamine
71523-78-9

Diacetamidopyrimethamine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With zinc(II) chloride In ethanol for 2h; Ambient temperature;
N-[5-(4-Chloro-phenyl)-2-(2,2-dimethyl-propionylamino)-6-ethyl-pyrimidin-4-yl]-2,2-dimethyl-propionamide
143947-40-4

N-[5-(4-Chloro-phenyl)-2-(2,2-dimethyl-propionylamino)-6-ethyl-pyrimidin-4-yl]-2,2-dimethyl-propionamide

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With zinc(II) chloride In ethanol for 2h; Heating;
Multi-step reaction with 3 steps
1: ZnCl2 / ethanol / 2 h / Heating
2: 76 percent / Heating
3: ZnCl2 / ethanol / 6 h / Heating
View Scheme
C26H21ClN4O2
143947-41-5

C26H21ClN4O2

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With zinc(II) chloride In ethanol for 6h; Heating;
Multi-step reaction with 3 steps
1: ZnCl2 / ethanol / 6 h / Heating
2: 62 percent / Heating
3: ZnCl2 / ethanol / 2 h / Heating
View Scheme
2-ethyl-6-chloro-5-<4-chloro-phenyl>-pyrimidin-2-ylamine

2-ethyl-6-chloro-5-<4-chloro-phenyl>-pyrimidin-2-ylamine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With ethanol; ammonia at 130℃;
sodium ethanolate
141-52-6

sodium ethanolate

<1-ethyl-2-<4-chloro-phenyl>-2-cyano-vinyl>-guanidine

<1-ethyl-2-<4-chloro-phenyl>-2-cyano-vinyl>-guanidine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With ethanol anschliessenden Erhitzen mit Guanidin in Aethanol auf 130grad/2 Torr;
guanidine nitrate
113-00-8

guanidine nitrate

α-(4-chlorophenyl)-β-methoxy-α-propionylacrylonitrile

α-(4-chlorophenyl)-β-methoxy-α-propionylacrylonitrile

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
In dimethyl sulfoxide at 80℃; for 0.0833333h;0.70 g
6-ethylisocytosine
5734-66-7

6-ethylisocytosine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 90 percent / POCl3 / Heating
2: 35 percent aq. NH3
3: 56 percent / I2; aq. NaOH / CHCl3 / 5 h
4: 76 percent / Pd(OAc)2(dppf)2; aq. K2HPO4 / 1,2-dimethoxy-ethane / 24 h / Heating
View Scheme
2,4-diamino-6-ethylpyrimidine
514854-12-7

2,4-diamino-6-ethylpyrimidine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 56 percent / I2; aq. NaOH / CHCl3 / 5 h
2: 76 percent / Pd(OAc)2(dppf)2; aq. K2HPO4 / 1,2-dimethoxy-ethane / 24 h / Heating
View Scheme
2-amino-4-chloro-6-ethylpyrimidine
5734-67-8

2-amino-4-chloro-6-ethylpyrimidine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 35 percent aq. NH3
2: 56 percent / I2; aq. NaOH / CHCl3 / 5 h
3: 76 percent / Pd(OAc)2(dppf)2; aq. K2HPO4 / 1,2-dimethoxy-ethane / 24 h / Heating
View Scheme
α-(4-chlorophenyl)-α-propionylacetonitrile
55474-40-3

α-(4-chlorophenyl)-α-propionylacetonitrile

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: dioxane / 20 °C
2: 0.70 g / dimethylsulfoxide / 0.08 h / 80 °C
View Scheme
Multi-step reaction with 2 steps
1: 100 °C
2: anschliessenden Erhitzen mit Guanidin in Aethanol auf 130grad/2 Torr
View Scheme
Multi-step reaction with 2 steps
1: toluene-4-sulfonic acid; toluene
2: ethanol
View Scheme
p-chlorobenzyl cyanide
140-53-4

p-chlorobenzyl cyanide

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: LDA / tetrahydrofuran / 0.17 h / -78 °C
1.2: 62 percent / tetrahydrofuran / -78 °C
2.1: dioxane / 20 °C
3.1: 0.70 g / dimethylsulfoxide / 0.08 h / 80 °C
View Scheme
Multi-step reaction with 3 steps
1: sodium ethylate
2: 100 °C
3: anschliessenden Erhitzen mit Guanidin in Aethanol auf 130grad/2 Torr
View Scheme
Multi-step reaction with 2 steps
1: sodium ethylate
2: diethyl ether / anschliessenden Erwaermen mit Guanidin in Aethanol
View Scheme
Multi-step reaction with 4 steps
1.1: sodium ethanolate / ethanol / 4 h / 80 °C
2.1: sodium hydride / tetrahydrofuran / 1.5 h / 0 - 20 °C / Inert atmosphere
2.2: 5 h / 0 - 20 °C / Inert atmosphere
3.1: sodium ethanolate / ethanol / 10 h / 80 °C
4.1: trifluoroacetic acid; acetic acid / acetonitrile / 0.17 h / 20 °C / Green chemistry
4.2: 10 h / 110 °C / 760.05 Torr / Green chemistry
View Scheme
2,4-diamino-5-<4-chloro-3-(3-methyltriazen-1-yl)phenyl>-6-ethylpyrimidine

2,4-diamino-5-<4-chloro-3-(3-methyltriazen-1-yl)phenyl>-6-ethylpyrimidine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 95 percent / 0.5M aq. HCl / 0.08 h / Heating
2: 1.) NaNO2, 5M aq. HCl; 2.) NaN3 / 1.) 0 deg C; 2.) 0 deg C, 2 h
3: 85 percent / 98percent hydrazine hydrate / 0.25 h / Heating
View Scheme
2,4-diamino-5-(3-amino-4-chlorophenyl)-6-ethylpyrimidine
24851-19-2

2,4-diamino-5-(3-amino-4-chlorophenyl)-6-ethylpyrimidine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1.) NaNO2, 5M aq. HCl; 2.) NaN3 / 1.) 0 deg C; 2.) 0 deg C, 2 h
2: 85 percent / 98percent hydrazine hydrate / 0.25 h / Heating
View Scheme
Multi-step reaction with 4 steps
1: 1.) 3M aq. HCl, aq. NaNO2 / 1.) 0 deg C; 2.) 0 deg C, 2 h
2: 95 percent / 0.5M aq. HCl / 0.08 h / Heating
3: 1.) NaNO2, 5M aq. HCl; 2.) NaN3 / 1.) 0 deg C; 2.) 0 deg C, 2 h
4: 85 percent / 98percent hydrazine hydrate / 0.25 h / Heating
View Scheme
Multi-step reaction with 2 steps
1: NaNO2, aq. HBF4
2: 64 percent / Et3N, formamide / Ambient temperature
View Scheme
2,4-diamino-5-(4-chloro-3-nitrophenyl)-6-ethylpyrimidine
21813-35-4

2,4-diamino-5-(4-chloro-3-nitrophenyl)-6-ethylpyrimidine

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: SnCl2*2H2O / ethanol / Heating
2: 1.) NaNO2, 5M aq. HCl; 2.) NaN3 / 1.) 0 deg C; 2.) 0 deg C, 2 h
3: 85 percent / 98percent hydrazine hydrate / 0.25 h / Heating
View Scheme
Multi-step reaction with 5 steps
1: SnCl2*2H2O / ethanol / Heating
2: 1.) 3M aq. HCl, aq. NaNO2 / 1.) 0 deg C; 2.) 0 deg C, 2 h
3: 95 percent / 0.5M aq. HCl / 0.08 h / Heating
4: 1.) NaNO2, 5M aq. HCl; 2.) NaN3 / 1.) 0 deg C; 2.) 0 deg C, 2 h
5: 85 percent / 98percent hydrazine hydrate / 0.25 h / Heating
View Scheme
N-[4-ethyl-5-(4-chloro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-2-yl]-acetamide
100709-69-1

N-[4-ethyl-5-(4-chloro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-2-yl]-acetamide

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: trichlorophosphate
2: ammonia; phenol / 110 °C
View Scheme
2-(4-chloro-phenyl)-3-oxo-propionitrile
62538-21-0

2-(4-chloro-phenyl)-3-oxo-propionitrile

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran / 1.5 h / 0 - 20 °C / Inert atmosphere
1.2: 5 h / 0 - 20 °C / Inert atmosphere
2.1: sodium ethanolate / ethanol / 10 h / 80 °C
3.1: trifluoroacetic acid; acetic acid / acetonitrile / 0.17 h / 20 °C / Green chemistry
3.2: 10 h / 110 °C / 760.05 Torr / Green chemistry
View Scheme
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

2,4-diamino-5-(4-chloro-3-nitrophenyl)-6-ethylpyrimidine
21813-35-4

2,4-diamino-5-(4-chloro-3-nitrophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
With sulfuric acid; nitric acid at 50℃; for 1h;95%
With sulfuric acid; nitric acid 50 deg C, 1 h; 25 deg C, 18 h;
With sulfuric acid; nitric acid
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

A

nitropyrimethamine

nitropyrimethamine

B

2,4-diamino-5-(4-chloro-3-nitrophenyl)-6-ethylpyrimidine
21813-35-4

2,4-diamino-5-(4-chloro-3-nitrophenyl)-6-ethylpyrimidine

Conditions
ConditionsYield
A n/a
B 93.8%
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

acetic anhydride
108-24-7

acetic anhydride

Diacetamidopyrimethamine
71523-78-9

Diacetamidopyrimethamine

Conditions
ConditionsYield
for 2h; Heating;89%
With acetic acid for 1.5h; Heating;57%
pentanoic anhydride
2082-59-9

pentanoic anhydride

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Pentanoic acid [5-(4-chloro-phenyl)-6-ethyl-2-pentanoylamino-pyrimidin-4-yl]-amide
143947-39-1

Pentanoic acid [5-(4-chloro-phenyl)-6-ethyl-2-pentanoylamino-pyrimidin-4-yl]-amide

Conditions
ConditionsYield
Heating;88%
6-bromo-2-phenyl-4H-benzo[2,3-d]-1,3-oxazin-4-one
66387-70-0

6-bromo-2-phenyl-4H-benzo[2,3-d]-1,3-oxazin-4-one

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

3-[4-amino-5-(4-chloro-phenyl)-6-ethyl-pyrimidin-2-yl]-6-bromo-2-phenyl-3H-quinazolin-4-one

3-[4-amino-5-(4-chloro-phenyl)-6-ethyl-pyrimidin-2-yl]-6-bromo-2-phenyl-3H-quinazolin-4-one

Conditions
ConditionsYield
In acetic acid for 6h; Heating;84%
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

propionic acid anhydride
123-62-6

propionic acid anhydride

N-[5-(4-Chloro-phenyl)-6-ethyl-2-propionylamino-pyrimidin-4-yl]-propionamide
143947-37-9

N-[5-(4-Chloro-phenyl)-6-ethyl-2-propionylamino-pyrimidin-4-yl]-propionamide

Conditions
ConditionsYield
Heating;83%
2-methyl-6-bromo-4H-3,1-benzoxazine-4-one
19165-25-4

2-methyl-6-bromo-4H-3,1-benzoxazine-4-one

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

3-[4-amino-5-(4-chloro-phenyl)-6-ethyl-pyrimidin-2-yl]-6-bromo-2-methyl-3H-quinazolin-4-one

3-[4-amino-5-(4-chloro-phenyl)-6-ethyl-pyrimidin-2-yl]-6-bromo-2-methyl-3H-quinazolin-4-one

Conditions
ConditionsYield
In acetic acid for 6h; Heating;83%
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

4-amino-6-ethyl-1,3,5-triazin-2-yl p-chlorophenyl ketone

4-amino-6-ethyl-1,3,5-triazin-2-yl p-chlorophenyl ketone

Conditions
ConditionsYield
With air; hematoporphyrin In ethanol for 7h; Irradiation;81%
With air; hematoporphyrin In ethanol for 7h; Product distribution; Mechanism; Irradiation; further solvents and sensitizens;
butanoic acid anhydride
106-31-0

butanoic acid anhydride

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

N-[2-Butyrylamino-5-(4-chloro-phenyl)-6-ethyl-pyrimidin-4-yl]-butyramide
143947-38-0

N-[2-Butyrylamino-5-(4-chloro-phenyl)-6-ethyl-pyrimidin-4-yl]-butyramide

Conditions
ConditionsYield
Heating;77%
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

benzoic acid anhydride
93-97-0

benzoic acid anhydride

C26H21ClN4O2
143947-41-5

C26H21ClN4O2

Conditions
ConditionsYield
Heating;76%
methanesulfonic acid
75-75-2

methanesulfonic acid

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

5-(4-chlorophenyl)-6-ethyl-2,4-pyrimidinediamine methane sulfonic acid

5-(4-chlorophenyl)-6-ethyl-2,4-pyrimidinediamine methane sulfonic acid

Conditions
ConditionsYield
In acetone at 20℃; for 1h; Solvent;70%
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

2,2-dimethylpropanoic anhydride
1538-75-6

2,2-dimethylpropanoic anhydride

N-[5-(4-Chloro-phenyl)-2-(2,2-dimethyl-propionylamino)-6-ethyl-pyrimidin-4-yl]-2,2-dimethyl-propionamide
143947-40-4

N-[5-(4-Chloro-phenyl)-2-(2,2-dimethyl-propionylamino)-6-ethyl-pyrimidin-4-yl]-2,2-dimethyl-propionamide

Conditions
ConditionsYield
Heating;62%
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

2-amino-5-(p-chlorophenyl)-t-6-ethyl-5,6-dihydro-r-5-hydroxy-4(3H)-pyrimidinone

2-amino-5-(p-chlorophenyl)-t-6-ethyl-5,6-dihydro-r-5-hydroxy-4(3H)-pyrimidinone

Conditions
ConditionsYield
With sodium tetrahydroborate; air; rose bengal In ethanol for 24h; Irradiation;39%
With sodium tetrahydroborate; air; rose bengal In ethanol for 24h; Mechanism; Irradiation;
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

acetic anhydride
108-24-7

acetic anhydride

A

acetyl-pyrimethamine
74124-11-1

acetyl-pyrimethamine

B

triacetyl-pyrimethamine
74124-12-2

triacetyl-pyrimethamine

Conditions
ConditionsYield
With pyridine Ambient temperature;A 31.5%
B 13%
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

2-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-4(3H)-one
91396-20-2

2-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-4(3H)-one

Conditions
ConditionsYield
With hydrogenchloride; water
With hydrogenchloride In water for 48h; Reflux; Inert atmosphere;
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

acetic anhydride
108-24-7

acetic anhydride

tetracetyl-pyrimethamine
74124-13-3

tetracetyl-pyrimethamine

Conditions
ConditionsYield
With pyridine Ambient temperature;
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

acetyl chloride
75-36-5

acetyl chloride

Diacetamidopyrimethamine
71523-78-9

Diacetamidopyrimethamine

Conditions
ConditionsYield
With dmap In pyridine for 12h; Ambient temperature;
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

A

2-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-4(3H)-one
91396-20-2

2-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-4(3H)-one

B

4-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-2(1H)-one
93456-61-2

4-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-2(1H)-one

Conditions
ConditionsYield
With hydrogenchloride In water for 18h; Heating;A 33 % Spectr.
B 67 % Spectr.
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

A

2-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-4(3H)-one hydrochloride
104498-88-6

2-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-4(3H)-one hydrochloride

B

4-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-2(1H)-one
93456-61-2

4-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-2(1H)-one

Conditions
ConditionsYield
With hydrogenchloride In water Product distribution; boiling, 18 h; 4 deg C, 6 d; further pyrimethamine derivatives, further reagent;A 33 % Spectr.
B 7 % Spectr.
2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine
58-14-0

2,4-diamino-5-(4-chlorophenyl)-6-ethylpyrimidine

Phenoxy-acetic acid (E)-10-oxo-dec-5-enyl ester

Phenoxy-acetic acid (E)-10-oxo-dec-5-enyl ester

Conditions
ConditionsYield
With sodium acetate; pyridinium chlorochromate In dichloromethane for 2h; Ambient temperature;

58-14-0Relevant articles and documents

Mechanochemical Magnesium-Mediated Minisci C-H Alkylation of Pyrimidines with Alkyl Bromides and Chlorides

Wu, Chongyang,Ying, Tao,Yang, Xinjie,Su, Weike,Dushkin, Alexandr V.,Yu, Jingbo

, p. 6423 - 6428 (2021/08/30)

A novel method to synthesize 4-alkylpyrimidines by the mechanochemical magnesium-mediated Minisci reaction of pyrimidine derivatives and alkyl halides has been reported. The reaction process operates with a broad substrate scope and excellent regioselectivity under mild conditions with no requirement of transition-metal catalysts, solvents, and inert gas protection. The practicality of this protocol has been demonstrated by the up-scale synthesis, mechanochemical product derivatization, and antimalarial drug pyrimethamine preparation.

Structure-based design, synthesis and preliminary evaluation of selective inhibitors of dihydrofolate reductase from Mycobacterium tuberculosis

El-Hamamsy, Mervat H.R.I.,Smith, Anthony W.,Thompson, Andrew S.,Threadgill, Michael D.

, p. 4552 - 4576 (2008/03/12)

Tuberculosis is an increasing threat, owing to the spread of AIDS and to the development of resistance of the causative organism, Mycobacterium tuberculosis, to the currently available drugs. Dihydrofolate reductase (DHFR) is an important enzyme of the folate cycle; inhibition of DHFR inhibits growth and causes cell death. The crystal structure of M. tuberculosis DHFR revealed a glycerol tightly bound close to the binding site for the substrate dihydrofolate; this glycerol-binding motif is absent from the human enzyme. A series of pyrimidine-2,4-diamines was designed with a two-carbon tether between a glycerol-mimicking triol and the 6-position of the heterocycle; these compounds also carried aryl substituents at the 5-position. These, their diastereoisomers, analogues lacking two hydroxy groups and analogues lacking the two-carbon spacing linker were synthesised by acylation of the anions derived from phenylacetonitriles with ethyl (4S,5R)-4-benzyloxymethyl-2,2-dimethyl-1,3-dioxolane-4-propanoate, ethyl (4S,5S)-4-benzyloxymethyl-2,2-dimethyl-1,3-dioxolane-4-propanoate, tetrahydrooxepin-2-one and 2,3-O-isopropylidene-d-erythronolactone, respectively, to give the corresponding α-acylphenylacetonitriles. Formation of the methyl enol ethers, condensation with guanidine and deprotection gave the pyrimidine-2,4-diamines. Preliminary assay of the abilities of these compounds to inhibit the growth of TB5 Saccharomyces cerevisiae carrying the DHFR genes from M. tuberculosis, human and yeast indicated that 5-phenyl-6-((3R,4S)-3,4,5-trihydroxypentyl)pyrimidine-2,4-diamine selectively inhibited M. tuberculosis DHFR and had little effect on the human or yeast enzymes.

Development of 2,4-diaminopyrimidines as antimalarials based on inhibition of the S108N and C59R+S108N mutants of dihydrofolate reductase from pyrimethamine resistant Plasmodium falciparum

Tarnchompoo, Bongkoch,Sirichaiwat, Chawanee,Phupong, Worrapong,Intaraudom, Chakapong,Sirawaraporn, Worachart,Kamchonwongpaisan, Sumalee,Vanichtanankul, Jarunee,Thebtaranonth, Yodhathai,Yuthavong, Yongyuth

, p. 1244 - 1252 (2007/10/03)

The reduced binding of pyrimethamine to Serl08Asn (S108N) mutants of parasite dihydrofolate reductase (DHFR), which forms the basis of resistance of Plasmodium falciparum to pyrimethamine, is largely due to steric constraint imposed by the bulky side chain of N108 on Cl of the 5-p-Cl-phenyl group. This and other S108 mutants with bulky side chains all showed reduced binding to pyrimethamine and cycloguanil. Less effect on binding to some bulky mutants was observed for trimethoprim, with greater flexibility for the 5-substituent. S108N DHFR also binds poorly with other pyrimethamine derivatives with bulky groups in place of the p-Cl, and the binding was generally progressively poorer for the double (C59R+S108N) mutant. Removal of the p-Cl or replacement with m-Cl led to better binding with the mutant DHFRs. Pyrimethamine analogues with unbranched hydrophobic 6-substituents showed generally good binding with the mutant DHFRs. A number of compounds were identified with high affinities for both wild-type and mutant DHFRs, with very low to no affinity to human DHFR. Some of these compounds show good antimalarial activities against pyrimethamine-resistant P. falciparum containing the mutant DHFRs with low cytotoxicity to three mammalian cell lines.

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