Benzenepropanoic acid → 5-Chloro-2-(2-phenylethyl)-1H-benzimidazole-6-sulfonamide
反応式
[NH2:1][C:2]1[CH:8]=[C:7]([Cl:9])[C:6]([S:10](=[O:13])(=[O:12])[NH2:11])=[CH:5][C:3]=1[NH2:4].[C:14](O)(=O)[CH2:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>Cl>[Cl:9][C:7]1[C:6]([S:10](=[O:12])(=[O:13])[NH2:11])=[CH:5][C:3]2[NH:4][C:14]([CH2:15][CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[N:1][C:2]=2[CH:8]=1参加物
実験手順
To 40 ml of 4 N hydrochloric acid containing 9.4 g of 2-amino-4-chloro-5-sulfamylaniline was added 9.5 g of hydrocinnamic acid and the mixture refluxed for 6 hours. The dark reaction mixture was concentrated in vacuo to a semi-solid which was then added with stirring to 200 ml of 38% ammonium hydroxide. After stirring for thirty minutes, the solid was collected by filtration and then suspended in 200 ml of water at 50° C. Upon stirring for thirty minutes, the product was collected by filtration, dissolved in methanol, and the solution treated with charcoal and boiled for five minutes. The suspension was cooled, filtered through Celite, and concentrated in vacuo to yield pink crystals. Recrystallization from acetonitrile provided 2.6 g of off-white crystals, mp 226°-228°.
後処理
- temperaturethe mixture refluxed for 6 hours
- customThe dark reaction mixture
- concentrationwas concentrated in vacuo to a semi-solid which
- additionwas then added
- stirringAfter stirring for thirty minutes
- filtrationthe solid was collected by filtration
- customsuspended in 200 ml of water at 50° C
- stirringUpon stirring for thirty minutes
- filtrationthe product was collected by filtration
- dissolutiondissolved in methanol
- additionthe solution treated with charcoal
- temperatureThe suspension was cooled
- filtrationfiltered through Celite
- concentrationconcentrated in vacuo
- customto yield pink crystals
- customRecrystallization from acetonitrile
出典と根拠
- ORDレコード
- ord-0713b0bd235d4f57b888492d5e9ca4f5
- 出典データセット
- uspto-grants-1983_12
- 特許番号
- US04420487
反応ノート
読み込み中…