[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]([NH2:11])[CH:3]=1.Cl.[Cl:13][C:14]1[CH:15]=[N:16][CH:17]=[CH:18][C:19]=1Cl>C(O)(C)C>[ClH:13].[Cl:13][C:14]1[CH:15]=[N:16][CH:17]=[CH:18][C:19]=1[NH:11][N:4]1[C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[C:2]([CH3:1])=[CH:3]1The title compound was prepared from 3-methyl-1H-indol-1-amine and 3,4-dichloropyridine hydrochloride in isopropanol at 80° C. for 5 hours in substantially the same manner as in Example 17. Recrystallized from ethanol, m.p. 278°-280° C. (dec.).
Wird geladen…