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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232721생성일: 2026년 10월 24일

Methyl chloroformate → 3,3a,4,5-tetrahydro-3a-methoxycarbonyl-N-[4'-(trifluoromethyl)phenyl]-2H-benz[g]indazole-2-carboxamide

https://huagongshe.com/ko/reaction/232721

반응식

참여 물질

역할이름HCID투입량
반응물Methyl chloroformateHCID 6586—
반응물DiisopropylamineHCID 7912—
반응물3,3a,4,5-Tetrahydro-N-[4-(trifluoromethyl)phenyl]-2H-benz[g]indazole-2-carboxamideHCID 23359467—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물3,3a,4,5-tetrahydro-3a-methoxycarbonyl-N-[4'-(trifluoromethyl)phenyl]-2H-benz[g]indazole-2-carboxamideHCID 18988349—

반응 조건

온도0 °C

반응 단계

To a solution of 0.9 ml of diisopropylamine in 10 ml of THF, at -78° C., was added 2.3 ml of 2.5M n-butyl lithium in hexane and the mixture was stirred for 5 mins. To this solution was added a solution of 1.0 g of the title compound of Step A in 5 ml of THF. The reaction was warmed to 0° C., recooled to -78° C. and then 0.75 ml of methyl chloroformate was added. The reaction mixture was then stirred for 24 h, with gradual warming to room temperature, quenched with 0.5 ml of glacial acetic acid, and poured into a 5% solution of aqueous NaHCO3. The mixture was extracted with chloroform, dried over magnesium sulfate and concentrated. Chromatography on silica gel with 30% ethyl acetate hexane afforded 0.25 g of the title compound, m.p. 177° to 180° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591764
출처 데이터셋uspto-grants-1997_01
ORD IDord-e5ea415d48054ca5aae5b4caae1d1dd0
출처 메모uspto-grants-1997_01