p-Hydrazinobenzenesulphonamide → Enflicoxib

HRID 1611860

反応式

HRID 1611860 の反応式
[O-]CC.[Na+].[F:5][C:6]([F:20])([F:19])[C:7](=O)[CH:8]=[CH:9][C:10]1[CH:15]=[CH:14][C:13]([F:16])=[CH:12][C:11]=1[F:17].[NH2:21][S:22]([C:25]1[CH:30]=[CH:29][C:28]([NH:31][NH2:32])=[CH:27][CH:26]=1)(=[O:24])=[O:23]>C(O)C>[NH2:21][S:22]([C:25]1[CH:26]=[CH:27][C:28]([N:31]2[CH:9]([C:10]3[CH:15]=[CH:14][C:13]([F:16])=[CH:12][C:11]=3[F:17])[CH2:8][C:7]([C:6]([F:20])([F:19])[F:5])=[N:32]2)=[CH:29][CH:30]=1)(=[O:24])=[O:23]

参加物

5

反応物 3

HCID 78105p-HydrazinobenzenesulphonamideHCID 2723922Sodium ethoxideHCID 69533569HCID 69533569、化合物

生成物 1

HCID 9953093Enflicoxib収率 65%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

In a flask with an inert atmosphere sodium ethoxide (0.53 g, 7.72 mmoles) is dissolved in 45 ml of ethanol. 1,1,1-trifluoro-4-(2,4-difluorophenyl)-3-butene-2-one (prepared according to method E-1) (0.913 g, 3.86 mmoles) and 4-(aminosulphonyl)phenylhydrazine chlorohydrate (0.87 g, 3.87 mmoles) are added and the mixture was refluxed for 16 hours. The mixture was cooled, evaporated to dryness, cold water added, and the mixture acidified by adding acetic acid and the precipitated solid filtered. This solid was redissolved in ether, treated with active C, filtered and the solvent eliminated with a rotavapor. The resulting residue was crystallised from ethyl ether-petrol ether (50:50) to give 1-(4-aminosulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole (1.02 g, yield: 65%) in the form of a solid m.p.=160-2° C.

後処理

  1. temperaturethe mixture was refluxed for 16 hours
  2. temperatureThe mixture was cooled
  3. customevaporated to dryness, cold water
  4. additionadded
  5. additionby adding acetic acid
  6. filtrationthe precipitated solid filtered
  7. dissolutionThis solid was redissolved in ether
  8. additiontreated with active C
  9. filtrationfiltered
  10. customThe resulting residue was crystallised from ethyl ether-petrol ether (50:50)

出典と根拠

ORDレコード
ord-35b3b07460ee4250b3e32f0a0adbd8ca
出典データセット
uspto-grants-2006_01
特許番号
USRE038963E1

関連ノート

読み込み中…