[CH3:1][C:2]1[S:15][C:5]2=[N:6][C:7]3[C:12]([C:13](=[O:14])[N:4]2[CH:3]=1)=[CH:11][CH:10]=[CH:9][CH:8]=3.[Cl:16][S:17](O)(=[O:19])=[O:18]>>[CH3:1][C:2]1[S:15][C:5]2=[N:6][C:7]3[C:12]([C:13](=[O:14])[N:4]2[CH:3]=1)=[CH:11][C:10]([S:17]([Cl:16])(=[O:19])=[O:18])=[CH:9][CH:8]=315 parts of 2-methyl-5H-thiazolo[2,3-b]quinazolin-5-one were introduced slowly into 70 parts of chlorosulfonic acid, at 20°-30° C. Stirring was continued for 12 hours, and the 2-methyl-7-chlorosulfonyl-5H-thiazolo[2,3-b]quinazolin-5-one formed was precipitated with ice water.
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