Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513841Generated: October 30, 2026

N-methyl-2-pyrrolidone → HCID 178432257, compound

https://huagongshe.com/reaction/513841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantAzane;hydrateHCID 12896473—
ReactantHCID 178418546HCID 178418546—
ReactantHCID 178432261HCID 178432261—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 178432257HCID 17843225789%

Reaction Steps

A mixture of 2-[5-amino-1-(2-methyl-1H-benzimidazol-5-yl)-1H-pyrazole-4-carbonyl]-1-(benzenesulfonyl)-5-iodo-1H-indole (117 mg), copper (I) cyanide (84 mg), and 1-methyl-2-pyrrolidinone was reacted in a microwave reactor (190° C., 20 minutes). The reaction mixture was poured into a mixed solution of 2 M ammonia water (40 ml), ethyl acetate (60 ml), and methanol (7 ml), and sonicated for five minutes. After ethyl acetate extraction, the extract was washed with water and then dried over anhydrous sodium sulfate. The desiccant was removed by filtration. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (methanol/dichloromethane=0/100 to 20/100) to give 2-[5-amino-1-(2-methyl-1H-benzimidazol-5-yl)-1H-pyrazole-4-carbonyl]-1-(benzenesulfonyl)-1H-indole-5-carbonitrile (87 mg, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102692B2
Source datasetuspto-grants-2015_08
ORD IDord-9fa1392f3f5147868f156aa6fffd1b0a
Source noteuspto-grants-2015_08