Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248372생성일: 2026년 10월 25일
Sodium hydride → 2-[N-butyryl-N-[4-(4-chloro-2-cyano-1-pyrrolyl)benzyl]amino]-4-methyl-3-nitropyridine
https://huagongshe.com/reaction/248372
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1-(4-Bromomethylphenyl)-4-chloropyrrole-2-carbonitrile | HCID 18961926 | — |
| 반응물 | 2-Butyrylamino-4-methyl-3-nitropyridine | HCID 21464239 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | 2-[N-butyryl-N-[4-(4-chloro-2-cyano-1-pyrrolyl)benzyl]amino]-4-methyl-3-nitropyridine | HCID 19759566 | — |
반응 단계
To a suspension of sodium hydride (114 mg, 60% oil dispersion) in dimethyl sulfoxide (5 ml) was added dropwise a solution of 2-butyrylamino-4-methyl-3-nitropyridine (605 mg) in dimethyl sulfoxide (10 ml) at ambient temperature under nitrogen atmosphere. The mixture was stirred at the same temperature for one hour and a solution of 1-(4-bromomethylphenyl)-4-chloropyrrole-2-carbonitrile (800 ml) in dimethyl sulfoxide (10 ml) was added therein. The reaction mixture was stirred at ambient temperature for 2 hours and quenched with ice water. The separated oil was extracted twice with ethyl acetate. The combined extracts were washed with water, dried, and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluted by n-hexane/ethylacetate (2/1-1/1) to yield 2-[N-butyryl-N-[4-(4-chloro-2-cyano-1-pyrrolyl)benzyl]amino]-4-methyl-3-nitropyridine (723 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05210092 |
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| 출처 데이터셋 | uspto-grants-1993_05 |
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| ORD ID | ord-3bca4c37b7a34ab79886e7008dd9a727 |
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| 출처 메모 | uspto-grants-1993_05 |
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