反応式
[CH3:1][O:2][C:3]1[CH:11]=[C:10]([S:12]([Cl:15])(=[O:14])=[O:13])[CH:9]=[CH:8][C:4]=1[C:5](O)=O.[CH3:16][NH:17][CH3:18].[NH2:19][C:20]1[C:25]([NH2:26])=[CH:24][N:23]=[CH:22][N:21]=1>>[ClH:15].[CH3:1][O:2][C:3]1[CH:11]=[C:10]([S:12]([N:17]([CH3:18])[CH3:16])(=[O:14])=[O:13])[CH:9]=[CH:8][C:4]=1[C:5]1[NH:26][C:25]2[C:20](=[N:21][CH:22]=[N:23][CH:24]=2)[N:19]=1参加物
4
実験手順
Prepared analogously to Example 51 from 2-methoxy-4-chlorosulfonyl-benzoic acid, aqueous dimethylamine solution, and 4,5-diamino-pyrimidine. The hydrochloride was recrystallized from ethanol/water (4:1).
後処理
- customThe hydrochloride was recrystallized from ethanol/water (4:1)
出典と根拠
- ORDレコード
- ord-124cdc4160634884ae47e8861d091964
- 出典データセット
- uspto-grants-1986_04
- 特許番号
- US04582837
関連ノート
読み込み中…