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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38756Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/38756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Isothiocyanato-2-(trifluoromethyl)benzonitrileHCID 11615540—
EduktAlanine, N-[4-(aminocarbonyl)-3-fluorophenyl]-2-methyl-, methyl esterHCID 66617687—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
ProduktN-DesmethylenzalutamideHCID 70678916—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524755B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-5e358dae823b4bd29d7a4dcebbbfc529
Quellennotizuspto-grants-2013_09