4-tert-Butylbenzoyl chloride → N4-(4-tert-butylbenzoyl)-N3-(4-methoxybenzoyl)-3,4-pyridinediamine
反応式
[C:1]([C:5]1[CH:13]=[CH:12][C:8]([C:9](Cl)=[O:10])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:14][O:15][C:16]1[CH:31]=[CH:30][C:19]([C:20]([NH:22][C:23]2[CH:24]=[N:25][CH:26]=[CH:27][C:28]=2[NH2:29])=[O:21])=[CH:18][CH:17]=1>>[C:1]([C:5]1[CH:13]=[CH:12][C:8]([C:9]([NH:29][C:28]2[CH:27]=[CH:26][N:25]=[CH:24][C:23]=2[NH:22][C:20](=[O:21])[C:19]2[CH:18]=[CH:17][C:16]([O:15][CH3:14])=[CH:31][CH:30]=2)=[O:10])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]参加物
3
実験手順
Using 4-tert-butylbenzoyl chloride and a similar procedure to that described for Example 2, Part C, N3-(4-methoxybenzoyl)-3,4-pyridinediamine (300 mg, 1.23 mmol) yielded 243 mg (49%) of the title compound.
出典と根拠
- ORDレコード
- ord-573ca34671054506ad38f76c16aa0c1c
- 出典データセット
- uspto-grants-2001_11