反応式
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]2[NH:6][N:7]=[N:8][C:4]=2[CH:3]=1.[OH:11][C:12]1[N:16]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[N:15]=[C:14]([CH3:23])[C:13]=1[N:24]=[N:25][C:26]1[CH:34]=[CH:33][C:29]([C:30](Cl)=[O:31])=[CH:28][CH:27]=1.CN(C)C1C=CC=CC=1.O>O1CCCC1>[NH:6]1[C:5]2[CH:9]=[CH:10][C:2]([NH:1][C:30](=[O:31])[C:29]3[CH:33]=[CH:34][C:26]([N:25]=[N:24][C:13]4[C:14]([CH3:23])=[N:15][N:16]([C:17]5[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=5)[C:12]=4[OH:11])=[CH:27][CH:28]=3)=[CH:3][C:4]=2[N:8]=[N:7]1参加物
6
実験手順
A mixture of 5-aminobenzotriazole (0.78 g), 4-(5-hydroxy-3-methyl-1-phenylpyrazol-4-ylazo)benzoyl chloride (2.0 g) and N,N-dimethylaniline (0.71 g) in dry tetrahydrofuran (15 ml) was stirred overnight and water (50 ml) was added. The precipitate was filtered and crystallized in aqueous pyridine (1.9 g), m.p. 285° decomp., λmax (methanol)=396 nm.
後処理
- filtrationThe precipitate was filtered
- customcrystallized in aqueous pyridine (1.9 g)
出典と根拠
- ORDレコード
- ord-861923de7ac74a1f8d42779d1685c841
- 出典データセット
- uspto-grants-1979_11
- 特許番号
- US04173478
関連ノート
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