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4858-85-9 Usage

Chemical Properties

clear colorless to light yellow liquid

Uses

Different sources of media describe the Uses of 4858-85-9 differently. You can refer to the following data:
1. 2,3-Dichloropyrazine is a substrate used for an efficient synthesis of aloisine (A575450), a potent cyclin-dependent kinase.
2. Selective monosubstitution of this substrate provided an efficient synthesis of alloisines, potent cyclin-dependent kinases.

Check Digit Verification of cas no

The CAS Registry Mumber 4858-85-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,5 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4858-85:
(6*4)+(5*8)+(4*5)+(3*8)+(2*8)+(1*5)=129
129 % 10 = 9
So 4858-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H2Cl2N2/c5-3-4(6)8-2-1-7-3/h1-2H

4858-85-9 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (L11500)  2,3-Dichloropyrazine, 98%   

  • 4858-85-9

  • 1g

  • 268.0CNY

  • Detail
  • Alfa Aesar

  • (L11500)  2,3-Dichloropyrazine, 98%   

  • 4858-85-9

  • 5g

  • 1002.0CNY

  • Detail
  • Aldrich

  • (465208)  2,3-Dichloropyrazine  95%

  • 4858-85-9

  • 465208-5G

  • 1,181.70CNY

  • Detail

4858-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Dichloropyrazine

1.2 Other means of identification

Product number -
Other names 2,3-Dichloro-1,4-diazine

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:4858-85-9 SDS

4858-85-9Synthetic route

2-chloropyrazin
14508-49-7

2-chloropyrazin

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

Conditions
ConditionsYield
Stage #1: 2-chloropyrazin With 2,2,6,6-tetramethyl-piperidine; n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h;
Stage #2: With hexachloroethane In tetrahydrofuran; hexane at -78℃; for 1h;
90%
With sulfuryl dichloride In N,N-dimethyl-formamide81%
2,3-dihydroxypirazine
931-18-0

2,3-dihydroxypirazine

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

Conditions
ConditionsYield
With trichlorophosphate84%
3-chloropyrazine 1-oxide
6863-76-9

3-chloropyrazine 1-oxide

A

2,5-dichloropyrazine
19745-07-4

2,5-dichloropyrazine

B

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

C

2,6-dichloropyrazine
4774-14-5

2,6-dichloropyrazine

Conditions
ConditionsYield
With trichlorophosphate for 2h; Heating; Yield given. Yields of byproduct given;
With 1,8-diazabicyclo[5.4.0]undec-7-ene; trichlorophosphate for 2h; Heating; Yield given. Yields of byproduct given;
Pyrazin-N.N'-dioxyd
2423-84-9

Pyrazin-N.N'-dioxyd

A

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

B

2,6-dichloropyrazine
4774-14-5

2,6-dichloropyrazine

Conditions
ConditionsYield
With trichlorophosphate for 2h; Heating; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
3-chloropyrazine 1-oxide
6863-76-9

3-chloropyrazine 1-oxide

A

2-chloropyrazin
14508-49-7

2-chloropyrazin

B

2,5-dichloropyrazine
19745-07-4

2,5-dichloropyrazine

C

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

D

2,6-dichloropyrazine
4774-14-5

2,6-dichloropyrazine

Conditions
ConditionsYield
With trichlorophosphate for 2h; Heating; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
2-chloropyrazine 1-oxide
16025-16-4

2-chloropyrazine 1-oxide

A

2-chloropyrazin
14508-49-7

2-chloropyrazin

B

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

C

2,6-dichloropyrazine
4774-14-5

2,6-dichloropyrazine

Conditions
ConditionsYield
With trichlorophosphate for 2h; Heating; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
2-chloropyrazin
14508-49-7

2-chloropyrazin

A

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

B

2,6-dichloro-pyrazine and 2,5-dichloro-pyrazine

2,6-dichloro-pyrazine and 2,5-dichloro-pyrazine

Conditions
ConditionsYield
With chlorine at 475℃;
1,4-pyrazine
290-37-9

1,4-pyrazine

water
7732-18-5

water

chlorine
7782-50-5

chlorine

A

2-chloropyrazin
14508-49-7

2-chloropyrazin

B

2,5-dichloropyrazine
19745-07-4

2,5-dichloropyrazine

C

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

D

2,6-dichloropyrazine
4774-14-5

2,6-dichloropyrazine

Conditions
ConditionsYield
at 350℃; Product distribution;
1,4-pyrazine
290-37-9

1,4-pyrazine

A

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

B

chloropyrazine, 2,6-dichloro-pyrazine, 2,5-dichloro-pyrazine

chloropyrazine, 2,6-dichloro-pyrazine, 2,5-dichloro-pyrazine

Conditions
ConditionsYield
With water; chlorine at 350℃;
With water; chlorine at 400 - 500℃;
With water; chlorine at 400 - 500℃;
3-chloropyrazine 1-oxide
6863-76-9

3-chloropyrazine 1-oxide

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

Conditions
ConditionsYield
With trichlorophosphate at 60℃; for 1h; Heating / reflux;
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

3-chloropyrazin-2-amine
6863-73-6

3-chloropyrazin-2-amine

Conditions
ConditionsYield
With ammonia In water at 100℃; for 18h; sealed tube;100%
With ammonium hydroxide In water at 100℃; for 24h;90%
With ammonium hydroxide In tetrahydrofuran at 100℃; for 18h;90%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

(3R)-3-Methyl-1-Tritylpiperazine
313657-75-9

(3R)-3-Methyl-1-Tritylpiperazine

(R)-1-(3-chloro-2-pyrazinyl)-2-methyl-4-tritylpiperazine
531503-76-1

(R)-1-(3-chloro-2-pyrazinyl)-2-methyl-4-tritylpiperazine

Conditions
ConditionsYield
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 127 - 133℃; for 41.5h;100%
With potassium carbonate In N,N-dimethyl-formamide at 100 - 110℃; for 20h;70.8%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

2-chloro-3-hydrazinopyrazine
63286-28-2

2-chloro-3-hydrazinopyrazine

Conditions
ConditionsYield
Stage #1: 2,3-dichloropyrazine With hydrazine hydrate In ethanol for 6h; Reflux;
Stage #2: With hydrazine hydrate In ethanol for 1h; Reflux;
100%
With hydrazine hydrate In ethanol; water Reflux;96%
With hydrazine In ethanol at 80℃; for 1h;93%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

2-phenoxyethanamine
1758-46-9

2-phenoxyethanamine

2-Chloro-3-(2-phenoxyethylamino)pyrazine
313654-73-8

2-Chloro-3-(2-phenoxyethylamino)pyrazine

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 180℃; for 0.333333h; microwave irradiation;100%
With potassium carbonate In hexane; ethyl acetate; acetonitrile2.36 g (49%)
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

2,4-Dimethoxybenzylamine
20781-20-8

2,4-Dimethoxybenzylamine

3-chloro-N-[(2,4-dimethoxyphenyl)methyl]pyrazin-2-amine
1190969-75-5

3-chloro-N-[(2,4-dimethoxyphenyl)methyl]pyrazin-2-amine

Conditions
ConditionsYield
100%
at 20℃; for 16h;
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

pinacol benzylboronate
87100-28-5

pinacol benzylboronate

2-benzyl-3-chloropyrazine
57693-15-9

2-benzyl-3-chloropyrazine

Conditions
ConditionsYield
With bis-triphenylphosphine-palladium(II) chloride; sodium carbonate In water; acetonitrile at 150℃; for 0.166667h; Inert atmosphere; Microwave irradiation;100%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

4-chloro-phenol
106-48-9

4-chloro-phenol

C9H5Cl2N3O

C9H5Cl2N3O

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 15h;100%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

4-chloro-phenol
106-48-9

4-chloro-phenol

2-chloro-3-(4-chlorophenoxy)pyrazine

2-chloro-3-(4-chlorophenoxy)pyrazine

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 15h;100%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

potassium tert-butylate
865-47-4

potassium tert-butylate

2-(tert-butoxy)-3-chloropyrazine

2-(tert-butoxy)-3-chloropyrazine

Conditions
ConditionsYield
In tetrahydrofuran for 1h; Inert atmosphere; Cooling with ice;100%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

m-tolylboronic acid
17933-03-8

m-tolylboronic acid

2,3-di-m-tolylpyrazine

2,3-di-m-tolylpyrazine

Conditions
ConditionsYield
Stage #1: 2,3-dichloropyrazine; m-tolylboronic acid With tetrakis(triphenylphosphine) palladium(0) In water; toluene at 95℃; for 0.166667h; Suzuki Coupling; Inert atmosphere;
Stage #2: With potassium fluoride dihydrate In water; toluene at 95℃; Suzuki Coupling; Inert atmosphere;
99%
With bis-triphenylphosphine-palladium(II) chloride; sodium carbonate In water; acetonitrile for 3.66667h;80%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

ditetrazolo<1,5-a:5',1'c>pyrazine
126229-04-7

ditetrazolo<1,5-a:5',1'c>pyrazine

Conditions
ConditionsYield
With sodium azide In dimethyl sulfoxide at 20℃; for 48h;98%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

Isobutyronitrile
78-82-0

Isobutyronitrile

2-(3-chloropyrazin-2-yl)-2-methylpropanenitrile

2-(3-chloropyrazin-2-yl)-2-methylpropanenitrile

Conditions
ConditionsYield
Stage #1: 2,3-dichloropyrazine With lithium hexamethyldisilazane In toluene
Stage #2: Isobutyronitrile In toluene at 20℃; for 24h;
98%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

propyl cyanide
109-74-0

propyl cyanide

2-(3-chloropyrazin-2-yl)butanenitrile
914360-89-7

2-(3-chloropyrazin-2-yl)butanenitrile

Conditions
ConditionsYield
Stage #1: 2,3-dichloropyrazine With lithium hexamethyldisilazane In toluene
Stage #2: propyl cyanide In toluene at 20℃; for 24h;
98%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

4-trifluoromethylphenylboronic acid
128796-39-4

4-trifluoromethylphenylboronic acid

2,3-bis(4-(trifluoromethyl)phenyl)pyrazine

2,3-bis(4-(trifluoromethyl)phenyl)pyrazine

Conditions
ConditionsYield
Stage #1: 2,3-dichloropyrazine; 4-trifluoromethylphenylboronic acid With tetrakis(triphenylphosphine) palladium(0) In water; toluene at 95℃; for 0.166667h; Suzuki Coupling; Inert atmosphere;
Stage #2: With potassium fluoride dihydrate In water; toluene at 95℃; Suzuki Coupling; Inert atmosphere;
98%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

phenylboronic acid
98-80-6

phenylboronic acid

2,3-diphenylpyrazine
1588-89-2

2,3-diphenylpyrazine

Conditions
ConditionsYield
Stage #1: 2,3-dichloropyrazine; phenylboronic acid With tetrakis(triphenylphosphine) palladium(0) In water; toluene at 95℃; for 0.166667h; Suzuki Coupling; Inert atmosphere;
Stage #2: With potassium fluoride dihydrate In water; toluene at 95℃; Suzuki Coupling; Inert atmosphere;
97%
With bis-triphenylphosphine-palladium(II) chloride; sodium carbonate In water; acetonitrile Suzuki coupling;74%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

4-methylphenylboronic acid
5720-05-8

4-methylphenylboronic acid

2,3-bis(p-methylphenyl)pyrazine
92405-82-8

2,3-bis(p-methylphenyl)pyrazine

Conditions
ConditionsYield
Stage #1: 2,3-dichloropyrazine; 4-methylphenylboronic acid With tetrakis(triphenylphosphine) palladium(0) In water; toluene at 95℃; for 0.166667h; Suzuki Coupling; Inert atmosphere;
Stage #2: With potassium fluoride dihydrate In water; toluene at 95℃; Suzuki Coupling; Inert atmosphere;
97%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

tert-butyl (1,3-cis)-N-(3-hydroxycyclobutyl)carbamate
389890-43-1

tert-butyl (1,3-cis)-N-(3-hydroxycyclobutyl)carbamate

tert-butyl ((1S,3S)-3-((3-chloropyrazin-2-yl)oxy)cyclobutyl)carbamate
1349184-47-9

tert-butyl ((1S,3S)-3-((3-chloropyrazin-2-yl)oxy)cyclobutyl)carbamate

Conditions
ConditionsYield
With caesium carbonate In dimethyl sulfoxide at 80℃;96.6%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

1-thiopropane
107-03-9

1-thiopropane

2-chloro-3-(propylthio)pyrazine
685872-18-8

2-chloro-3-(propylthio)pyrazine

Conditions
ConditionsYield
With sodium hydroxide In ethanol at 20℃; for 2h;96%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

butyrophenone
495-40-9

butyrophenone

2-(3-chloropyrazin-2-yl)-1-phenylbutan-1-one
914360-74-0

2-(3-chloropyrazin-2-yl)-1-phenylbutan-1-one

Conditions
ConditionsYield
Stage #1: 2,3-dichloropyrazine With lithium hexamethyldisilazane In toluene
Stage #2: propiophenone In toluene at 60℃; for 24h;
96%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

sulfanilamide
63-74-1

sulfanilamide

4-amino-N-(3-chloro-pyrazin-2-yl)-benzenesulfonamide
14423-79-1

4-amino-N-(3-chloro-pyrazin-2-yl)-benzenesulfonamide

Conditions
ConditionsYield
With potassium carbonate In N-methyl-acetamide; water; toluene95%
With potassium carbonate
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

acetonitrile
75-05-8

acetonitrile

(3-chloropyrazin-2-yl)acetonitrile

(3-chloropyrazin-2-yl)acetonitrile

Conditions
ConditionsYield
Stage #1: 2,3-dichloropyrazine With lithium hexamethyldisilazane In toluene
Stage #2: acetonitrile In toluene at 20℃; for 24h;
95%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

N-aminopyridin-1-ium iodide
6295-87-0

N-aminopyridin-1-ium iodide

N-(3'-chloropyrazin-2'-yl)pyridinium aminide

N-(3'-chloropyrazin-2'-yl)pyridinium aminide

Conditions
ConditionsYield
With potassium carbonate In acetonitrile for 20h; Heating;95%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

1-tert-Butyl 4-methyl piperidine-1,4-dicarboxylate
124443-68-1

1-tert-Butyl 4-methyl piperidine-1,4-dicarboxylate

1-tert-butyl 4-methyl 4-(3-chloropyrazin-2-yl)piperidine-1,4-dicarboxylate
1227068-50-9

1-tert-butyl 4-methyl 4-(3-chloropyrazin-2-yl)piperidine-1,4-dicarboxylate

Conditions
ConditionsYield
With lithium hexamethyldisilazane In tetrahydrofuran at 20℃; for 16h; Inert atmosphere;95%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

2-amino-benzenethiol
137-07-5

2-amino-benzenethiol

10H-benzo[b]pyrazino[2,3-e][1,4]thiazine
37693-82-6

10H-benzo[b]pyrazino[2,3-e][1,4]thiazine

Conditions
ConditionsYield
With potassium hydroxide In water; N,N-dimethyl-formamide for 4h; Heating;94%
With sodium carbonate In 1,2-dichloro-benzene Heating;
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

1,1'-bis[4-(dimethylamino)(pyrazine-2,3-diyl)pyridinium]dichloride

1,1'-bis[4-(dimethylamino)(pyrazine-2,3-diyl)pyridinium]dichloride

Conditions
ConditionsYield
In 1,2-dichloro-benzene at 140℃; for 1h;94%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

4-aminomethyl-piperidine-1-carboxylic acid benzyl ester
157023-34-2

4-aminomethyl-piperidine-1-carboxylic acid benzyl ester

benzyl 4-{[(3-chloropyrazin-2-yl)amino]methyl}piperidine-1-carboxylate
455265-59-5

benzyl 4-{[(3-chloropyrazin-2-yl)amino]methyl}piperidine-1-carboxylate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In isopropyl alcohol for 72h; Heating;94%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

4-fluoroboronic acid
1765-93-1

4-fluoroboronic acid

2,3-bis(4-fluorophenyl)pyrazine
909567-96-0

2,3-bis(4-fluorophenyl)pyrazine

Conditions
ConditionsYield
Stage #1: 2,3-dichloropyrazine; 4-fluoroboronic acid With tetrakis(triphenylphosphine) palladium(0) In water; toluene at 95℃; for 0.166667h; Suzuki Coupling; Inert atmosphere;
Stage #2: With potassium fluoride dihydrate In water; toluene at 95℃; Suzuki Coupling; Inert atmosphere;
94%
1,3 dithiane
505-23-7

1,3 dithiane

2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

methyl iodide
74-88-4

methyl iodide

2-chloro-3-(2-methyl-1,3-dithian-2-yl)pyrazine
1131041-56-9

2-chloro-3-(2-methyl-1,3-dithian-2-yl)pyrazine

Conditions
ConditionsYield
Stage #1: 1,3 dithiane With n-butyllithium In tetrahydrofuran at -20℃; for 1h;
Stage #2: methyl iodide In tetrahydrofuran at -50 - 20℃;
Stage #3: 2,3-dichloropyrazine With n-butyllithium In tetrahydrofuran at -50 - 20℃;
93%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

diphenylamine
122-39-4

diphenylamine

5-phenyl-5H-pyrazino[2,3-b]indole
1202362-87-5

5-phenyl-5H-pyrazino[2,3-b]indole

Conditions
ConditionsYield
With palladium diacetate; sodium t-butanolate; tricyclohexylphosphine In toluene at 105℃; for 18h; Inert atmosphere; regioselective reaction;93%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

methylamine
74-89-5

methylamine

3-chloro-N-methylpyrazin-2-amine

3-chloro-N-methylpyrazin-2-amine

Conditions
ConditionsYield
In ethanol at 80℃; for 0.5h; Inert atmosphere; Sealed tube;93%
In tetrahydrofuran; dichloromethane43.6%
In tetrahydrofuran at 20℃; for 24h;43.6%

4858-85-9Relevant articles and documents

Synthesis of pyrazine alcaloids from Botryllus leachi. diazines 43

Buron, Frederic,Ple, Nelly,Turck, Alain,Queguiner, Guy

, p. 2616 - 2621 (2007/10/03)

(Chemical Equation Presented) Regioselective metalation of pyrazines and cross-coupling reactions provides an easy access to botryllazines A and B and to an isomer of botryllazine A with good yields from chloropyrazine.

Heterocyclic-ring condensed benzothiazine compound

-

, (2008/06/13)

The invention provides a novel heterocyclic ring condensed benzothiazine compound which is effective for prevention or remedy of disease, in which histamine, leukotriene and the like participate. The heterocyclic ring condensed benzothiazine compound of the present invention or a pharmacologically acceptable salt thereof is effective for prevention or remedy of disease, in which a chemical mediator, such as histamine, leukotriene and the like, participate, for example, asthma, allergic coryza, atopic dermatitis, hives, hay fever, gastrointestinal allergy, food allergy and the like. Further, the heterocyclic ring condensed benzothiazine compound of the present invention, its pharmacologically acceptable salt or hydrates thereof is represented by the following formula: In the formula, the ring Het represents an unsaturated heterocyclic ring; R1and R2are the same as or different from each other, and each represents halogen atom, a lower alkyl group that may be substituted with a halogen atom, a lower alkoxy group that may be substituted with a halogen atom, a lower alkyl lower alkoxy group, cyano group; D represents a lower alkylene group and the like that may have a substituent; Q represents, for example, the formula —NR20R2(in the formula, R20and R21are the same as or different from each other, and each represents hydrogen atom, a lower alkyl group that may be substituted with a halogen atom, an aryl group that may have a substituent, an arylalkyl group that may have a substituent, a heteroaryl group that may have a substituent or a heteroarylalkyl group that may have a substituent, or R20and R21may form a 3- to 8-membered ring along with the nitrogen atom to which they are bound); and x represents an integer of from 1 to 2.

Synthesis of Derivatives of Pyrazinopyridimidin-4-ones

Dennin, F.,Blondeau, D.,Sliwa, H.

, p. 1639 - 1643 (2007/10/02)

3-Alkoxy-2-aminopyrazines have been condensed with ethyl ethoxymethylenemalonate and isopropylidene methoxymethylenemalonate to afford 9-alkoxypyrazinopyrimidin-4-ones substituted in the first case by an ethoxycarbonyl group at 3 position.

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