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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38756Generated: October 25, 2026

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

https://huagongshe.com/reaction/38756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Isothiocyanato-2-(trifluoromethyl)benzonitrileHCID 11615540—
ReactantAlanine, N-[4-(aminocarbonyl)-3-fluorophenyl]-2-methyl-, methyl esterHCID 66617687—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductN-DesmethylenzalutamideHCID 70678916—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524755B2
Source datasetuspto-grants-2013_09
ORD IDord-5e358dae823b4bd29d7a4dcebbbfc529
Source noteuspto-grants-2013_09