5-AMINO-3-CHLOROPYRAZINE-2-CARBONITRILE

Base Information

• Chemical Name: 5-AMINO-3-CHLOROPYRAZINE-2-CARBONITRILE
• CAS No.: 34617-65-7
• Molecular Formula: C5H3ClN4
• Molecular Weight: 154.559
• Hs Code.: 2933990090
• Mol file: 34617-65-7.mol

Synonyms:5-AMINO-3-CHLORO-2-PYRAZINECARBONITRILE;5-amino-3-chloro-pyrazine-2-carbonitrile;

Chemical Property of 5-AMINO-3-CHLOROPYRAZINE-2-CARBONITRILE

Chemical Property:

• PSA: 75.59000
• LogP: 1.16508

Purity/Quality:

97% ^*data from raw suppliers

5-?Amino-?3-?chloropyrazine-?2-?carbonitrile ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: 5-?Amino-?3-?chloropyrazine-?2-?carbonitrile is a reagent used in the synthesis of orally bioavailable CHK1 inhibitors.

Technology Process of 5-AMINO-3-CHLOROPYRAZINE-2-CARBONITRILE

There total 7 articles about 5-AMINO-3-CHLOROPYRAZINE-2-CARBONITRILE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

zinc(II) cyanide (557-21-1) + 6-chloro-5-iodo-pyrazin-2-ylamine (925678-00-8) → 5-amino-3-chloro-pyrazine-2-carbonitrile (34617-65-7)

Guidance literature:

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1-methyl-pyrrolidin-2-one; at 100 ℃; for 14h;

Reference yield: 84.0%

6-chloro-5-iodo-pyrazin-2-ylamine (925678-00-8) → 5-amino-3-chloro-pyrazine-2-carbonitrile (34617-65-7)

Guidance literature:

In N,N-dimethyl-formamide; at 150 ℃; for 2h;

Reference yield: 84.0%

6-chloro-5-iodo-pyrazin-2-ylamine (925678-00-8) + copper(l) cyanide → 5-amino-3-chloro-pyrazine-2-carbonitrile (34617-65-7)

Guidance literature:

In N,N-dimethyl-formamide; at 150 ℃; for 2h;

upstream raw materials:

5-amino-3-chloro-pyrazine-2-carbaldehyde O-acetyl-oxime

2-chloro-3-bromo-6-aminopyrazine

zinc(II) cyanide

6-chloro-5-iodo-pyrazin-2-ylamine

Downstream raw materials:

3-(4-fluorophenyl)-6-((3-(pyridin-4-yloxy)azetidin-1-yl)methyl)imidazo[1,5-a]pyrazin-8(7H)-one

N-(2-(allyloxy)-5-chloro-4-{[2-(trimethylsilyl)ethoxy]methoxy}phenyl)-N'-[6-(but-3-enyloxy)-5-cyanopyrazin-2-yl]urea

N-[2-(allyloxy)-5-chlorophenyl]-N'-[6-(allyloxy)-5-cyanopyrazin-2-yl]urea

N-[2-(allyloxy)-5-chlorophenyl]-N'-[6-(3-butenyloxy)-5-cyano-2-pyrazinyl]urea