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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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-(4-Bromomethylphenyl)-4-chloropyrrole-2-carbonitrileHCID 18961926—
반응물2-Butyrylamino-4-methyl-3-nitropyridineHCID 21464239—
용매Dimethyl SulfoxideHCID 679—
생성물2-[N-butyryl-N-[4-(4-chloro-2-cyano-1-pyrrolyl)benzyl]amino]-4-methyl-3-nitropyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210092
출처 데이터셋uspto-grants-1993_05
ORD IDord-3bca4c37b7a34ab79886e7008dd9a727
출처 메모uspto-grants-1993_05