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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74454Generated: October 30, 2026

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

https://huagongshe.com/reaction/74454

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 numberUS08829199B2
Source datasetuspto-grants-2014_09
ORD IDord-7f4a445e6e354b8ca6233dd93c3c46fa
Source noteuspto-grants-2014_09