[S:1]1[C:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:4]=2[CH:3]=[C:2]1[C:10]([NH2:12])=[O:11].[Cl:13][CH2:14][C:15]([CH2:17]Cl)=O>>[Cl:13][CH2:14][C:15]1[N:12]=[C:10]([C:2]2[S:1][C:5]3[CH2:6][CH2:7][CH2:8][CH2:9][C:4]=3[CH:3]=2)[O:11][CH:17]=1In substantially the same manner as in Reference Example 47, 4,5,6,7-tetrahydro-2-benzothiophene carboxamide was allowed to react with 1,3-dichloroacetone to give 4-chloromethyl-2-(4,5,6,7-tetrahydro-2-benzothienyl)oxazole. The yield was 53%. Recrystallization from ethyl acetate-hexane gave colorless needles, mp 102-103° C.
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