Benzenepropanoic acid → 5-Chloro-2-(2-phenylethyl)-1H-benzimidazole-6-sulfonamide
반응식
[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]=1참가 물질
실험 절차
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°.
후처리
- 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
출처 및 근거
- ORD 기록
- ord-0713b0bd235d4f57b888492d5e9ca4f5
- 출처 데이터셋
- uspto-grants-1983_12
- 특허 번호
- US04420487
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