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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1353생성일: 2026년 10월 23일

Water → 6-(4-Nitrobenzoyl)-2,3-dimethyl-3,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepine

https://huagongshe.com/ko/reaction/1353

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물HCID 178418238HCID 178418238—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
생성물6-(4-Nitrobenzoyl)-2,3-dimethyl-3,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepineHCID 69955561—

반응 단계

In a stream of argon, 144 mg of 60% sodium hydride was suspended in a small volume of N,N-dimethylformamide to which, with cooling on an ice bath, was then added dropwise a solution prepared by dissolving 500 mg of 6-(4-nitrobenzoyl)-2-methyl-1,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepine in 20 ml of N,N-dimethylformamide. After 1 hour of stirring at room temperature, the reaction solution was mixed with 0.11 ml of methyl iodide and stirred for 24 hours at room temperature. The reaction solution was mixed with water and chloroform, and the resulting organic layer was separated, washed with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. After removing the solvent by distillation under a reduced pressure, the thus obtained residue was subjected to silica gel column chromatography to obtain 351 mg of 6-(4-nitrobenzoyl)-2,3-dimethyl-3,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepine from the chloroform-methyl alcohol (30:1) eluate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723606
출처 데이터셋uspto-grants-1998_03
ORD IDord-a3bb18217e0f4155870b6f9c59379a87
출처 메모uspto-grants-1998_03