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ChemicalBook CAS DataBase List Enzalutamide
1242137-17-2

Enzalutamide synthesis

1synthesis methods
N-desMethyl EnzalutaMide

1242137-16-1
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Enzalutamide

1242137-17-2
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-

Yield:-

Reaction Conditions:

with dihydrogen peroxide in ethanol;water; for 1 h;Reflux;

Steps:

7

To a solution of 4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2- thioxoimidazolidin-l-yl)-2-fluorobenzamide (Compound (MII)) (1.48 g, 3.4 mmol) in ethanol (60 mL) was added 30% aqueous H2O2 (30 mL) at room temperature. The solution was heated to reflux for 1 h. After removal of ethanol, brine (100 mL) was added and the aqueous layer was extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated under reduced pressure to obtain the crude product that was purified by silica gel chromatography. MS (m/z): 435 (M+l). HPLC: Column, YMC ODS A, 4.6x150 mm, 5 m, Mobile Phase A: 10 mM Ammonium acetate, Mobile Phase B: Acetonitrile, Gradient, 10% B up to 2 min, 10% to 90% B in 6 min, hold for 10 min, 90% to 10% B in 4 min, Retention time, 9.548 min, HPLC Purity, 98.08%, Flow Rate, 1 mL/min. 1H NMR (CDCl3, Freebase): d (ppm) 8.3 (t, IH), 8.18 (s, IH), 8.2 (d, IH), 7.96 (d, IH), 7.25 (m, 2H), 6.65 (bd, IH), 5.9 (bs, IH) 1.65 (s, 6H).

References:

WO2010/99238,2010,A1 Location in patent:Page/Page column 35

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