Sulfanilic acid → 4-(6-Chloro-4-quinazolinylamino)benzenesulphonic acid
反応式
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Cl:12])[CH:10]=2)[N:5]=[CH:4][N:3]=1.[S:13]([OH:23])(=[O:22])([C:15]1[CH:20]=[CH:19][C:18]([NH2:21])=[CH:17][CH:16]=1)=[O:14]>C(O)C>[Cl:12][C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][CH:8]=1)[N:5]=[CH:4][N:3]=[C:2]2[NH:21][C:18]1[CH:19]=[CH:20][C:15]([S:13]([OH:23])(=[O:14])=[O:22])=[CH:16][CH:17]=1参加物
4
実験手順
4,6-Dichloroquinazoline (5.9 g, 0.03 mole) was added portionwise to sulphanilic acid (5.2 g, 0.03 mole) in 50% aqueous ethanol (200 ml) at 90° C. with stirring. The mixture was refluxed for 2 hours, cooled and filtered. The solid was washed with 50% aqueous ethanol and dried in an oven to give the title compound (9.2 g) as the hemihydrate m.p. greater than 300° C.
後処理
- temperatureThe mixture was refluxed for 2 hours
- temperaturecooled
- filtrationfiltered
- washThe solid was washed with 50% aqueous ethanol
- customdried in an oven
出典と根拠
- ORDレコード
- ord-cc34361490594b21a045245fd81b2432
- 出典データセット
- uspto-grants-1987_02
- 特許番号
- US04640920
反応ノート
読み込み中…