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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71139생성일: 2026년 10월 23일

Triethylamine → tert-butyl 2-{[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]carbonyl}hydrazinecarboxylate

https://huagongshe.com/ko/reaction/71139

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-Butyl carbazateHCID 70091—
반응물DiethylphosphorylcyanideHCID 13586794—
반응물3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoic acidHCID 57931763—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물tert-butyl 2-{[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]carbonyl}hydrazinecarboxylateHCID 6660867344.3%

반응 단계

To a mixture of 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzoic acid (12.1 g) and tert-butyl hydrazinecarboxylate (7.61 g) in DMF (100 mL) was added diethyl phosphoryl cyanide (8.55 mL) at room temperature. After stirring at room temperature for 30 min, triethylamine (21.6 mL) was added, and the mixture was stirred overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (8.00 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822699B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3792cda2947945bb985eb21bbdc96d17
출처 메모uspto-grants-2014_09