[F:1][C:2]1[CH:9]=[CH:8][C:5](C=O)=[CH:4][CH:3]=1.[C:10]1([CH3:17])[C:15]([SH:16])=[CH:14][CH:13]=[CH:12][CH:11]=1.[CH:18]([NH2:20])=[O:19].[C:21]1(C)C=CC=CC=1>CCOC(C)=O.O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:20]([CH2:21][S:16][C:15]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[CH3:17])[CH:18]=[O:19])=[CH:8][CH:9]=1A solution of p-fluorobenzaldehyde (13.1 milliliters (hereinafter mL), 122 millimoles (hereinafter mmol) thiocresol (16.64 grams (hereinafter g), 122 mmol), formamide (15.0 mL, 445 mmol), and toluene (300 mL) were combined and heated to toluene reflux with azeotropic removal of H2O for 18 h. The cooled reaction was diluted with EtOAc (500 mL) and washed with said aq Na2CO3 (3×100 mL), said aq NaCl (100 mL), dried (Na2SO4), and concentrated. The residue was triturated with petroleum ether, filtered and dried in vacuo to afford 28.50 g of the title compound as a white solid (85%) melting point (hereinafter mp) =119°-120°.
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