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4472-44-0

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4472-44-0 Usage

Uses

2-Chloro-4,6-dimethylpyrimidine is a chlorinated pyrimidine with antiviral activity.

Check Digit Verification of cas no

The CAS Registry Mumber 4472-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,7 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4472-44:
(6*4)+(5*4)+(4*7)+(3*2)+(2*4)+(1*4)=90
90 % 10 = 0
So 4472-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H7ClN2/c1-4-3-5(2)9-6(7)8-4/h3H,1-2H3

4472-44-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H50331)  2-Chloro-4,6-dimethylpyrimidine, 99%   

  • 4472-44-0

  • 250mg

  • 555.0CNY

  • Detail
  • Alfa Aesar

  • (H50331)  2-Chloro-4,6-dimethylpyrimidine, 99%   

  • 4472-44-0

  • 1g

  • 2000.0CNY

  • Detail
  • Aldrich

  • (708445)  2-Chloro-4,6-dimethylpyrimidine  97%

  • 4472-44-0

  • 708445-25G

  • 3,348.54CNY

  • Detail

4472-44-0Synthetic route

4,6-dimethyl-2-hydroxy-pyrimidine hydrochloride
34289-60-6

4,6-dimethyl-2-hydroxy-pyrimidine hydrochloride

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

Conditions
ConditionsYield
With trichlorophosphate for 10h; Inert atmosphere; Reflux;91%
With trichlorophosphate for 10h; Heating;77%
With trichlorophosphate for 10h; Reflux;77%
With trichlorophosphate In neat (no solvent) for 10h; Inert atmosphere; Reflux;77%
2-oxo-4,6-dimethyl-1,2-dihydropyrimidine hydrochloride
34289-60-6

2-oxo-4,6-dimethyl-1,2-dihydropyrimidine hydrochloride

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

Conditions
ConditionsYield
With trichlorophosphate for 18h; Heating / reflux;56%
With trichlorophosphate
lighter-than-water

lighter-than-water

4,6-dimethyl-2(1H)-pyrimidinone
108-79-2

4,6-dimethyl-2(1H)-pyrimidinone

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

Conditions
ConditionsYield
In diethyl ether; trichlorophosphate55%
4-amino-1-[9,10-dihydro-9,10-methanoanthracen-9-ylmethyl]piperidine
149605-42-5

4-amino-1-[9,10-dihydro-9,10-methanoanthracen-9-ylmethyl]piperidine

A

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

B

2-[1-(9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidylamino]-4,6-dimethylpyrimidine
771447-77-9

2-[1-(9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidylamino]-4,6-dimethylpyrimidine

Conditions
ConditionsYield
A n/a
B 55%
4,6-dimethyl-2(1H)-pyrimidinone
108-79-2

4,6-dimethyl-2(1H)-pyrimidinone

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

Conditions
ConditionsYield
With trichlorophosphate for 23h; Heating / reflux;55%
benzylamine
100-46-9

benzylamine

4,6-dimethyl-2-meraptopyrimidine
22325-27-5

4,6-dimethyl-2-meraptopyrimidine

A

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

B

N-benzyl-4,6-dimethylpyrimidine-2-sulfonamide

N-benzyl-4,6-dimethylpyrimidine-2-sulfonamide

Conditions
ConditionsYield
Stage #1: 4,6-dimethyl-2-meraptopyrimidine With hydrogenchloride; sodium hypochlorite In dichloromethane; water at -10 - -5℃; for 0.25h;
Stage #2: benzylamine In dichloromethane at 0℃; for 0.5h;
A n/a
B 19%
1-benzyl-3,5-dimethyl-1H-pyrazole
1134-81-2

1-benzyl-3,5-dimethyl-1H-pyrazole

chloroform
67-66-3

chloroform

A

2-chloro-4-methylpyrimidine
13036-57-2

2-chloro-4-methylpyrimidine

B

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

C

2-phenylpyrimidine
7431-45-0

2-phenylpyrimidine

D

4,6-dimethyl-2-phenylpyrimidine
14164-34-2

4,6-dimethyl-2-phenylpyrimidine

Conditions
ConditionsYield
at 550 - 555℃; Further byproducts given. Title compound not separated from byproducts;
1-benzyl-3,5-dimethyl-1H-pyrazole
1134-81-2

1-benzyl-3,5-dimethyl-1H-pyrazole

chloroform
67-66-3

chloroform

A

2-chloro-4-methylpyrimidine
13036-57-2

2-chloro-4-methylpyrimidine

B

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

C

4,6-dimethyl-2-phenylpyrimidine
14164-34-2

4,6-dimethyl-2-phenylpyrimidine

D

3-Methylpyrazole
1453-58-3

3-Methylpyrazole

Conditions
ConditionsYield
at 550 - 555℃; Further byproducts given. Title compound not separated from byproducts;
1-benzyl-3,5-dimethyl-1H-pyrazole
1134-81-2

1-benzyl-3,5-dimethyl-1H-pyrazole

A

NH-pyrazole
288-13-1

NH-pyrazole

B

2-chloro-4-methylpyrimidine
13036-57-2

2-chloro-4-methylpyrimidine

C

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

D

4,6-dimethyl-2-phenylpyrimidine
14164-34-2

4,6-dimethyl-2-phenylpyrimidine

Conditions
ConditionsYield
With chloroform at 550 - 555℃; Further byproducts given. Title compound not separated from byproducts;
1-benzyl-3,5-dimethyl-1H-pyrazole
1134-81-2

1-benzyl-3,5-dimethyl-1H-pyrazole

A

2-chloro-4-methylpyrimidine
13036-57-2

2-chloro-4-methylpyrimidine

B

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

C

4,6-dimethyl-2-phenylpyrimidine
14164-34-2

4,6-dimethyl-2-phenylpyrimidine

D

3-Methylpyrazole
1453-58-3

3-Methylpyrazole

Conditions
ConditionsYield
With chloroform at 550 - 555℃; Further byproducts given. Title compound not separated from byproducts;
hydrogenchloride
7647-01-0

hydrogenchloride

4,6-dimethylpirimidin-2-one
108-79-2

4,6-dimethylpirimidin-2-one

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

hydrochloride of 2-oxy-4.6-dimethyl-pyrimidine

hydrochloride of 2-oxy-4.6-dimethyl-pyrimidine

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

Conditions
ConditionsYield
With trichlorophosphate
2-Amino-4,6-dimethylpyrimidine
767-15-7

2-Amino-4,6-dimethylpyrimidine

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

Conditions
ConditionsYield
With hydrogenchloride; sodium nitrite
With hydrogenchloride; zinc(II) chloride; sodium nitrite In dichloromethane; water
With hydrogenchloride; zinc(II) chloride; sodium nitrite In dichloromethane; water
acetylacetone
123-54-6

acetylacetone

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: ethanol / Heating
2: aq. NaNO2; HCl
View Scheme
Multi-step reaction with 2 steps
1: hydrogenchloride / ethanol; water / 24 h / Inert atmosphere; Reflux
2: trichlorophosphate / 10 h / Inert atmosphere; Reflux
View Scheme
Multi-step reaction with 2 steps
1: hydrogenchloride
2: trichlorophosphate / Reflux
View Scheme
Multi-step reaction with 2 steps
1: hydrogenchloride / ethanol / 3 h / Heating / reflux
2: trichlorophosphate / 18 h / Heating / reflux
View Scheme
Multi-step reaction with 2 steps
1: hydrogenchloride
2: trichlorophosphate / Reflux
View Scheme
acetylacetone
123-54-6

acetylacetone

CH2=CH(CH2)3-halide

CH2=CH(CH2)3-halide

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 75 percent / conc. HCl / ethanol / 24 h / Heating
2: 77 percent / phosphorus oxychloride / 10 h / Heating
View Scheme
4,6-dimethyl-2(1H)-pyrimidinone
108-79-2

4,6-dimethyl-2(1H)-pyrimidinone

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

Conditions
ConditionsYield
With trichlorophosphate for 1h; Heating / reflux;
With sodium hydroxide In trichlorophosphate
With sodium bicarbonate; trichlorophosphate In water
4,6-dimethylpirimidin-2-one
108-79-2

4,6-dimethylpirimidin-2-one

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

Conditions
ConditionsYield
With trichlorophosphate
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

p-toluidine
106-49-0

p-toluidine

4,6-dimethyl-N-(4-methylphenyl)-2-pyrimidinamine
81261-68-9

4,6-dimethyl-N-(4-methylphenyl)-2-pyrimidinamine

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;99%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

4-bromo-aniline
106-40-1

4-bromo-aniline

N-(4-bromophenyl)-4,6-dimethyl-2-pyrimidinamine
81261-71-4

N-(4-bromophenyl)-4,6-dimethyl-2-pyrimidinamine

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;98%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

sodium diphenylphosphinodithioate
5827-17-8

sodium diphenylphosphinodithioate

diphenyl (4,6-dimethyl-2-pyrimidyl) dithiophosphinate
24625-65-8

diphenyl (4,6-dimethyl-2-pyrimidyl) dithiophosphinate

Conditions
ConditionsYield
In toluene for 9h; Condensation; Heating;98%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

4-phenyl-1-piperazine
92-54-6

4-phenyl-1-piperazine

4,6-dimethyl-2-(4-phenylpiperazin-1-yl)pyrimidine

4,6-dimethyl-2-(4-phenylpiperazin-1-yl)pyrimidine

Conditions
ConditionsYield
With C50H61Cl2N3Pd; potassium tert-butylate In 1,4-dioxane at 100℃; for 2h;97%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

decylthiol
143-10-2

decylthiol

2-(decylthio)-4,6-dimethylpyrimidine

2-(decylthio)-4,6-dimethylpyrimidine

Conditions
ConditionsYield
Stage #1: decylthiol With 18-crown-6 ether; potassium hydroxide In tetrahydrofuran; water for 2h; Reflux;
Stage #2: 2-chloro-4,6-dimethylpyrimidine In tetrahydrofuran; water for 24h; Reflux;
97%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

3-aminobenzenemethanol
1877-77-6

3-aminobenzenemethanol

{3-[(4,6-dimethylpyrimidine-2-yl)-amino]-phenyl}-methanol

{3-[(4,6-dimethylpyrimidine-2-yl)-amino]-phenyl}-methanol

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;97%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

meta-fluoroaniline
372-19-0

meta-fluoroaniline

N-(3-fluorophenyl)-4,6-dimethyl-2-pyrimidinamine

N-(3-fluorophenyl)-4,6-dimethyl-2-pyrimidinamine

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;97%
piperazine
110-85-0

piperazine

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

1-(4,6-dimethyl-pyrimidin-2-yl)piperazine
22746-09-4

1-(4,6-dimethyl-pyrimidin-2-yl)piperazine

Conditions
ConditionsYield
With potassium carbonate In tetrahydrofuran; water at 20℃; for 24h;96%
In dimethyl sulfoxide at 100℃; for 16h;93%
Stage #1: piperazine With potassium carbonate In water at 45 - 50℃; for 4.5h; Inert atmosphere;
Stage #2: 2-chloro-4,6-dimethylpyrimidine In water at 20℃; Inert atmosphere;
93%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

2-benzyloctahydropyrrolo[3,4-c]pyrrole
86732-22-1

2-benzyloctahydropyrrolo[3,4-c]pyrrole

2-benzyl-5-(4,6-dimethyl-pyrimidin-2-yl )-octahydro-pyrrolo[3,4-c]pyrrole
1293284-73-7

2-benzyl-5-(4,6-dimethyl-pyrimidin-2-yl )-octahydro-pyrrolo[3,4-c]pyrrole

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 100℃; for 15h;96%
With caesium carbonate In N,N-dimethyl-formamide at 100℃; for 15h; Inert atmosphere;96%
1-methyl-piperazine
109-01-3

1-methyl-piperazine

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

4,6-dimethyl-2-(4-methylpiperazin-1-yl)pyrimidine
903433-02-3

4,6-dimethyl-2-(4-methylpiperazin-1-yl)pyrimidine

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 50℃; for 72h;96%
In N,N-dimethyl-formamide at 90℃; for 2.5h; Inert atmosphere;93%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

cis-3-benzyl-3,7-diazabicyclo[3.3.0]octane
172739-04-7

cis-3-benzyl-3,7-diazabicyclo[3.3.0]octane

2-benzyl-5-(4,6-dimethylpyrimidin-2-yl)octahydropyrrolo[3,4-c]pyrrole

2-benzyl-5-(4,6-dimethylpyrimidin-2-yl)octahydropyrrolo[3,4-c]pyrrole

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 100℃; for 15h; Inert atmosphere;96%
methanol
67-56-1

methanol

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

2-methoxy-4,6-dimethylpyrimidine
14001-61-7

2-methoxy-4,6-dimethylpyrimidine

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran; mineral oil for 2h;96%
morpholine
110-91-8

morpholine

2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

4-(4,6-dimethylpyrimidin-2-yl)morpholine
7749-51-1

4-(4,6-dimethylpyrimidin-2-yl)morpholine

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 90℃; for 2.5h; Inert atmosphere;95%
at 210℃; for 0.166667h; Microwave irradiation;92%
With ethanol
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

benzylamine
100-46-9

benzylamine

N-benzyl-2-amino-4,6-dimethylpyrimidine
106270-42-2

N-benzyl-2-amino-4,6-dimethylpyrimidine

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;95%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

isopropyl alcohol
67-63-0

isopropyl alcohol

2-isopropoxy-4,6-dimethylpyrimidine

2-isopropoxy-4,6-dimethylpyrimidine

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran; mineral oil for 2h;95%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

pentan-1-ol
71-41-0

pentan-1-ol

4,6-dimethyl-2-(pentyloxy)pyrimidine

4,6-dimethyl-2-(pentyloxy)pyrimidine

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran; mineral oil for 1h;94%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

ethanol
64-17-5

ethanol

2-ethoxy-4,6-dimethylpyrimidine
7781-21-7

2-ethoxy-4,6-dimethylpyrimidine

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran; mineral oil for 3h;94%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

4-amino-phenol
123-30-8

4-amino-phenol

4-[(4,6-dimethylpyrimidine-2-yl)-amino]-phenol

4-[(4,6-dimethylpyrimidine-2-yl)-amino]-phenol

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;92%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

aniline
62-53-3

aniline

Pyrimethanil
53112-28-0

Pyrimethanil

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;91%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

trimethylamine
75-50-3

trimethylamine

(4,6-dimethylpyrimid-2′-yl)-trimethylammonium chloride
77767-94-3

(4,6-dimethylpyrimid-2′-yl)-trimethylammonium chloride

Conditions
ConditionsYield
In benzene 1) 0 deg C; 2) room temperature, 1h;91%
In water at 0℃;88%
With benzene
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

4-Aminobiphenyl
92-67-1

4-Aminobiphenyl

N-(biphenyl-4-yl)-4,6-dimethyl-2-pyrimidinamine

N-(biphenyl-4-yl)-4,6-dimethyl-2-pyrimidinamine

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;91%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

4-Aminoazobenzene
60-09-3

4-Aminoazobenzene

4,6-dimethyl-N-{4-[(E)-phenyldiazenyl]-phenyl}-2-pyrimidinamine

4,6-dimethyl-N-{4-[(E)-phenyldiazenyl]-phenyl}-2-pyrimidinamine

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;91%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

4-methoxy-aniline
104-94-9

4-methoxy-aniline

N-(4-methoxylphenyl)-4,6-dimethyl-2-pyrimidinamine
23951-85-1

N-(4-methoxylphenyl)-4,6-dimethyl-2-pyrimidinamine

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;90%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

3,4,5-Trimethoxyaniline
24313-88-0

3,4,5-Trimethoxyaniline

4,6-dimethyl-N-(3,4,5-trimethoxyphenyl)-2-pyrimidinamine

4,6-dimethyl-N-(3,4,5-trimethoxyphenyl)-2-pyrimidinamine

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;90%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

o-toluidine
95-53-4

o-toluidine

4,6-dimethyl-N-(2-methylphenyl)-2-pyrimidinamine

4,6-dimethyl-N-(2-methylphenyl)-2-pyrimidinamine

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;90%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

bis(4-aminophenyl)disulfide
722-27-0

bis(4-aminophenyl)disulfide

N,N'-[dithiobis(4,1-phenylene)]bis(4,6-dimethylpyrimidin-2-amine)

N,N'-[dithiobis(4,1-phenylene)]bis(4,6-dimethylpyrimidin-2-amine)

Conditions
ConditionsYield
In ethanol at 160℃; for 0.166667h; Microwave irradiation; Sealed tube; Green chemistry;90%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

2-(methoxymethyl)-4-(piperazin-1-yl)pyrimidine
300553-61-1

2-(methoxymethyl)-4-(piperazin-1-yl)pyrimidine

2-methoxymethyl-4-[4-(4,6-dimethyl-pyrimidinin-2-yl)-piperazin-1-yl]-pyrimidine
400784-91-0

2-methoxymethyl-4-[4-(4,6-dimethyl-pyrimidinin-2-yl)-piperazin-1-yl]-pyrimidine

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In butan-1-ol Heating;89%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

phenylmagnesium chloride
100-59-4

phenylmagnesium chloride

4,6-dimethyl-2-phenylpyrimidine
14164-34-2

4,6-dimethyl-2-phenylpyrimidine

Conditions
ConditionsYield
With quinoline; ferric(III) bromide In tetrahydrofuran; tert-butyl methyl ether at 25℃; for 0.0833333h; Reagent/catalyst; Inert atmosphere;89%
With ferric(III) bromide In tetrahydrofuran; tert-butyl methyl ether at 20℃; for 2h; Inert atmosphere; Schlenk technique;76%
2-chloro-4,6-dimethylpyrimidine
4472-44-0

2-chloro-4,6-dimethylpyrimidine

tributyl(thien-2-yl)stannane
54663-78-4

tributyl(thien-2-yl)stannane

4,6-dimethyl-2-(thiophen-2-yl)pyrimidine
67945-74-8

4,6-dimethyl-2-(thiophen-2-yl)pyrimidine

Conditions
ConditionsYield
With potassium carbonate; bis-triphenylphosphine-palladium(II) chloride; tetraethylammonium chloride In N,N-dimethyl-formamide at 110℃; for 2h;88%

4472-44-0Relevant articles and documents

Solvatochromic behavior of a pyrene-pyrimidine-based Schiff base and detection of heavy metal ions in aqueous media

Ghosh, Swadesh,Singharoy, Dipti,Konar, Saugata,Naskar, Jnan Prakash,Bhattacharya, Subhash Chandra

, p. 1272 - 1283 (2021/03/26)

The synthesis and solvatochromic behavior of pyrimidine based Schiff-base (PYPH) were studied to develop a fluorescent chemo sensor for the detection of Hg2+ in aqueous solution. The characterization of PYPH was investigated on the basis of UV–vis, FTIR, 1H-NMR and mass spectral data. PYPH displays selective fluorescent turn-off response to Hg2+ in aqueous solution. The sensitivity and selectivity of PYPH toward Hg2+ among different metal ions was examined by absorption, fluorescence, 1H-NMR and mass spectral studies. Binding stoichiometry (2:1) has been confirmed by a Job’s plot, HRMS spectral studies and 1H-NMR analysis. A low detection limit was 4.2 × 10?6 M for Hg2+. Ground state geometry of PYPH has been optimized using density functional theory (DFT). These results demonstrate that PYPH has promise to detect Hg2+ ion in environmental analysis systems.

Nonionic Surfactants as Potential Carriers of a Synthesized Pyrimidine Derivative: Spectroscopic and Quantum Chemical Investigations

Ghosh, Swadesh,Singharoy, Dipti,Dhara, Anamika,Naskar, Jnan Prakash,Bhattacharya, Subhash Chandra

, p. 2695 - 2701 (2018/06/27)

Currently, a major problem is the poor water solubility and bioavailability of many pharmaceuticals. Using different types of surfactants is an effective strategy to overcome this problem. Herein a pyrimidine-based Schiff base, 2-[2-(anthracen-9-ylmethylene) hydrazinyl]-4,6-dimethyl pyrimidine (ANHP), has been synthesized and characterized by different spectroscopic methods. A comparative study of drug carrier properties of cationic, anionic, and the nonionic surfactants with this pyrimidine derivative (ANHP) in aqueous solution is the key research interest of this work. From fluorescence studies, the interaction of ANHP with the different types of surfactants were compared and binding constants of ANHP in vesicles were determined. The drug carrier properties of different surfactants were investigated by using different spectroscopic techniques. DLS, zeta potential, and AFM studies have shown that in the presence of ANHP, nonionic surfactants take a vesicular shape. Several experimental results clearly indicate that Ig-720 is the better choice as ANHP carrier among all the surfactants investigated. In addition, the structure of ANHP has been optimized by density functional theory (DFT). The theoretical and experimental results have been compared.

Synthesis and biological activity of novel dimethylpyrazole and piperazine-containing (bis)1,2,4-triazole derivatives

Wang, Bao-Lei,Zhang, Yan,Liu, Xing-Hai,Zhang, Li-Yuan,Zhan, Yi-Zhou,Zhang, Xiao,Wang, Li-Zhong,Li, Yong-Hong,Li, Zheng-Ming

, p. 34 - 41 (2016/12/24)

A series of novel dimethylpyrazole and piperazine-containing (bis)1,2,4-triazole derivatives have been conveniently synthesized via Mannich reaction in good yields. Their structures were identified by IR,1H NMR,13C NMR, and elemental analysis. The preliminary bioassays showed that among 14 new compounds, the trifluoromethyl-containing compounds exhibited superior activity than the methyl-containing ones; some of the compounds displayed significant in vitro and in vivo fungicidal activity against several plant fungi and were comparable with the control Triadimefon; several compounds exhibited certain herbicidal activity against Brassica campestris; several compounds possessed favorable KARI inhibitory activity, especially 8D could be a promising KARI inhibitor for further study. The research results will provide useful information for the design and discovery of new agrochemicals with novel heterocyclic Mannich base structures containing piperazine moiety.

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