Acetic Anhydride → N,3-bis-(4-chlorophenyl)-4-dimethylcarbamoyl-4-methyl-N-acetyl-4,5-dihydro-1H-pyrazole-1-carboxamide

HRID 1607226ノート

反応式

HRID 1607226 の反応式
[H-].[Na+].[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:11]([N:13]2[CH2:17][C:16]([C:19](=[O:23])[N:20]([CH3:22])[CH3:21])([CH3:18])[C:15]([C:24]3[CH:29]=[CH:28][C:27]([Cl:30])=[CH:26][CH:25]=3)=[N:14]2)=[O:12])=[CH:6][CH:5]=1.[H][H].[C:33](OC(=O)C)(=[O:35])[CH3:34]>O1CCCC1>[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([N:10]([C:33](=[O:35])[CH3:34])[C:11]([N:13]2[CH2:17][C:16]([C:19](=[O:23])[N:20]([CH3:22])[CH3:21])([CH3:18])[C:15]([C:24]3[CH:25]=[CH:26][C:27]([Cl:30])=[CH:28][CH:29]=3)=[N:14]2)=[O:12])=[CH:6][CH:5]=1

参加物

6

実験手順

In a 50 ml round bottomed flask was placed 0.45 g of 60% sodium hydride (0.011 mole). The sodium hydride was washed twice with hexane and suspended in 15 ml of tetrahydrofuran. A solution of 2.0 g (0.005 mole) of N,3-bis-(4-chlorophenyl)-4-dimethylcarbamoyl-4-methyl-4,5-dihydro-1H-pyrazole-1-carboxamide in 5 ml of tetrahydrofuran was added slowly. When hydrogen evolution ceased, 1 ml of acetic anhydride was added and the mixture was stirred for 5 minutes. The reaction was partitioned between ethyl ether and brine, dried, concentrated, and chromatographed yielding 1.6 g of N,3-bis-(4-chlorophenyl)-4-dimethylcarbamoyl-4-methyl-N-acetyl-4,5-dihydro-1H-pyrazole-1-carboxamide, an oil. NMR and IR data were consistent with the structure.

後処理

  1. customIn a 50 ml round bottomed flask was placed
  2. washThe sodium hydride was washed twice with hexane
  3. customThe reaction was partitioned between ethyl ether and brine
  4. customdried
  5. concentrationconcentrated
  6. customchromatographed

出典と根拠

ORDレコード
ord-84f8a79c6a5142be8e63a230c8000b99
出典データセット
uspto-grants-1989_09
特許番号
US04863947

反応ノート

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