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HRID 38756作成日:2026年10月26日

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

https://huagongshe.com/reaction/38756

反応式

関与物質

役割名称HCID仕込み量
反応物4-Isothiocyanato-2-(trifluoromethyl)benzonitrileHCID 11615540—
反応物Alanine, N-[4-(aminocarbonyl)-3-fluorophenyl]-2-methyl-, methyl esterHCID 66617687—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物N-DesmethylenzalutamideHCID 70678916—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524755B2
出典データセットuspto-grants-2013_09
ORD IDord-5e358dae823b4bd29d7a4dcebbbfc529
出典メモuspto-grants-2013_09