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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501639생성일: 2026년 10월 24일

(2R,3R)-3-(tert-Butyl-dimethylsilanyloxy)-2-[(1R)-(2,2,2-trifluoro-1-hydroxyethyl)]pyrrolidine-1-carboxylic acid tert-butyl ester → (1S,7R,7aR)-2-Trifluoromethyl-4-(7-hydroxy-1-trifluoromethyl-3-oxohexahydropyrrolo[1,2-c]imidazol-2-yl)-3-methylbenzonitrile

https://huagongshe.com/ko/reaction/501639

반응식

참여 물질

역할이름HCID투입량
반응물(2R,3R)-3-(tert-Butyl-dimethylsilanyloxy)-2-[(1R)-(2,2,2-trifluoro-1-hydroxyethyl)]pyrrolidine-1-carboxylic acid tert-butyl esterHCID 16732286—
반응물4-Cyano-2-methyl-3-trifluoromethylphenyl isocyanateHCID 59754272—
생성물(1S,7R,7aR)-2-Trifluoromethyl-4-(7-hydroxy-1-trifluoromethyl-3-oxohexahydropyrrolo[1,2-c]imidazol-2-yl)-3-methylbenzonitrileHCID 59754290—

반응 단계

The title compound was prepared from (2R,3R)-3-(tert-butyl-dimethylsilanyloxy)-2-[(1R)-(2,2,2-trifluoro-1-hydroxyethyl)]pyrrolidine-1-carboxylic acid tert-butyl ester (66A) and isocyanate 18E following procedures analogous to those found in Example 72. LCMS: m/z 394 [M+H]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772267B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-b715b9bd83c64c0ab2ea7af6f18b74a5
출처 메모uspto-grants-2010_08