Benzenepropanoic acid → 5-Chloro-2-(2-phenylethyl)-1H-benzimidazole-6-sulfonamide

HRID 904850ノート

反応式

HRID 904850 の反応式
[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

4

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

  1. temperaturethe mixture refluxed for 6 hours
  2. customThe dark reaction mixture
  3. concentrationwas concentrated in vacuo to a semi-solid which
  4. additionwas then added
  5. stirringAfter stirring for thirty minutes
  6. filtrationthe solid was collected by filtration
  7. customsuspended in 200 ml of water at 50° C
  8. stirringUpon stirring for thirty minutes
  9. filtrationthe product was collected by filtration
  10. dissolutiondissolved in methanol
  11. additionthe solution treated with charcoal
  12. temperatureThe suspension was cooled
  13. filtrationfiltered through Celite
  14. concentrationconcentrated in vacuo
  15. customto yield pink crystals
  16. 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

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