Malononitrile → HCID 178488016, 화합물

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CO[C:3]1[CH:18]=[CH:17][C:6]2[N:7]=[C:8]([NH:10][N:11]=[C:12]([C:15]#[N:16])[C:13]#[N:14])[S:9][C:5]=2[CH:4]=1.[C:19](#N)CC#N.[OH2:24].[NH2:25][NH2:26]>C(O)C>[NH2:16][C:15]1[C:12](=[N:11][NH:10][C:8]2[S:9][C:5]3[CH:4]=[C:3]([O:24][CH3:19])[CH:18]=[CH:17][C:6]=3[N:7]=2)[C:13]([NH2:14])=[N:26][N:25]=1

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실험 절차

This compound was prepared using 2-[(6-methoxybenzothiazol-2-yl)hydrazono]-malononitrile (200 mg), which was derived from 2-amino-6-methoxybensothiazole (1.17 g) and malononitrile (0.82 g) as described in Example 8, and hydrazine hydrate (0.2 mL) in ethanol. Solids had not formed after heating the reaction at 40° C. for 2 hrs. The solution was allowed to cool to room temperature and concentrated. The product was obtained after column chromatography purification (80 mg, 35%).