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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38756생성일: 2026년 10월 24일

4-Isothiocyanato-2-(trifluoromethyl)benzonitrile → N-Desmethylenzalutamide

https://huagongshe.com/ko/reaction/38756

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참여 물질

역할이름HCID투입량
반응물4-Isothiocyanato-2-(trifluoromethyl)benzonitrileHCID 11615540—
반응물Alanine, N-[4-(aminocarbonyl)-3-fluorophenyl]-2-methyl-, methyl esterHCID 66617687—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물N-DesmethylenzalutamideHCID 70678916—

반응 단계

A solution of methyl 2-(4-carbamoyl-3-fluorophenylamino)-2-methylpropanoate and 2-(trifluoromethyl)-4-isothiocyanatobenzonitrile (1.5 equivalents) in dry DMSO (5 mL per mmol) was heated to 80-82° C. for 12 h. The reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layer was concentrated under reduced pressure and the residue was purified by silica gel chromatography eluting with 40% Acetone-Hexanes. MS (m/z): 451 (M+1). HPLC: Column, YMC ODS A, 4.6×150 mm, 5 μm, Mobile Phase A:10 mM Ammonium acetate, Mobile Phase B: Acetonitrile, Gradient, 10% B up to 2 min, 10% to 90% B in 3 min, hold for 3 min, 90% to 10% B in 5 min, Retention time, 2.782 min, HPLC Purity, 99.4%, Flow Rate, 1 mL/min. 1H NMR (CDCl3, Freebase): δ (ppm) 8.3 (t, 1H), 8.0 (d, 1H) 7.98 (s, 1H), 7.8 (d, 1H), 7.27 (d, 1H), 7.2 (d, 1H), 6.65 (d, 1H), 6.0 (s, 1H), 1.62 (s,6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524755B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5e358dae823b4bd29d7a4dcebbbfc529
출처 메모uspto-grants-2013_09