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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25074생성일: 2026년 10월 26일

Dimethylformamide → (R)-N'-(8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-7-carbothioyl)-acetic hydrazide

https://huagongshe.com/reaction/25074

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물AcetohydrazideHCID 14039—
반응물(R)-8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-7-carbothioyl chlorideHCID 12137405—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
생성물(R)-N'-(8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-7-carbothioyl)-acetic hydrazideHCID 86593813—

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온도50 °C

반응 단계

To a solution of 4.04 g (10.0 mmol) of the starting material XII, 3 ml of dimethylformamide, 1.40 ml (10.0 mmol) of triethylamine and 0.06 g (0.5 mmol) of 4-dimethylaminopyridine 1.48 g (20.0 mmol) of acetic hydrazide was added. The reaction mixture was stirred at 50° C. for 5 h, then diluted with water, the precipitated crystals were filtered off and washed with water. The so obtained 4.5 g of (R)—N′-{8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-7-carbothioyl}-acetic hydrazide according to its 1H-NMR spectrum was a mixture of rotation isomers. (The analyzed sample was purified by column chromatography using a mixture of n-hexane-ethyl acetate (1:1) as eluent and it was crystallized with 0.5 mol of ethyl acetate, Mp.: 118° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858605B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-aca65a8d2fc7443881e36f7679c978c1
출처 메모uspto-grants-2005_02