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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42633생성일: 2026년 10월 24일

Water → N-[(1S)-1-(4-{3-[2,6-bis(trifluoromethyl)pyridin-4-yl]-3-(trifluoromethyl)pyrrolidin-1-yl}phenyl)ethyl]cyclopropanecarboxamide

https://huagongshe.com/ko/reaction/42633

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물N-[(1S)-1-(4-bromophenyl)ethyl]cyclopropanecarboxamideHCID 800360—
반응물Sodium t-butoxideHCID 23676156—
반응물2,6-Bis(trifluoromethyl)-4-[3-(trifluoromethyl)pyrrolidin-3-yl]pyridineHCID 53262187—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
용매TolueneHCID 1140—
생성물N-[(1S)-1-(4-{3-[2,6-bis(trifluoromethyl)pyridin-4-yl]-3-(trifluoromethyl)pyrrolidin-1-yl}phenyl)ethyl]cyclopropanecarboxamideHCID 53261994100.9%

반응 단계

To the solution of N-[(1S)-1-(4-bromophenyl)ethyl]cyclopropanecarboxamide (0.134 g) and 2,6-bis(trifluoromethyl)-4-[3-(trifluoromethyl)pyrrolidin-3-yl]pyridine (0.195 g) in toluene was added sodium tert-butoxide (0.096 g), tris(dibenzylideneacetone)dipalladium chloroform complex (0.010 g) and xantphos (0.017 g) and the vessel was applied by Ar gas. The vessel was sealed and applied to microwave reactor at 120° C. for 10 min. The mixture was cooled to room temperature and then poured into water, which was then extracted twice with ethyl acetate. The organic layer was combined, which was then washed with water and dried over anhydrous magnesium sulfate. After the drying agent was filtered off, the solvent was distilled away under the reduced pressure, and the residue was then purified by silica gel chromatography to yield N-[(1S)-1-(4-{3-[2,6-bis(trifluoromethyl)pyridin-4-yl]-3-(trifluoromethyl)pyrrolidin-1-yl}phenyl)ethyl]cyclopropanecarboxamide (0.272 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536201B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-8c9ab98ad9934ccd8557d2e19c071ef0
출처 메모uspto-grants-2013_09