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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Reactant | HCID 178432261 | HCID 178432261 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178432257 | HCID 178432257 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102692B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-9fa1392f3f5147868f156aa6fffd1b0a |
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| Source note | uspto-grants-2015_08 |
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