COC(C1CC2C(=CC=C(S)C=2)C1)=O.[CH3:15][O:16][C:17](=[O:47])[CH2:18][N:19]1[CH2:28][CH2:27][C:26]2[C:21](=[CH:22][CH:23]=[C:24]([S:29]CC3SC(C4C=CC(C(F)(F)F)=CC=4)=NC=3C)[CH:25]=2)[CH2:20]1>>[CH3:15][O:16][C:17](=[O:47])[CH2:18][N:19]1[CH2:28][CH2:27][C:26]2[C:21](=[CH:22][CH:23]=[C:24]([SH:29])[CH:25]=2)[CH2:20]110C was prepared analogously to compound 1C. 74% yield. MS: 238 (M+1)+. Preparation of {6-[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethylsulfanyl]-3,4-dihydro-1H-isoquinolin-2-yl}-acetic acid methyl ester (Compound 10D)
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