tert-Butanol → N-(tert-Butoxycarbonyl)-[1-(2,4-dichlorophenyl)-5-(4-chlorophenyl)-1H-pyrazol-3-yl]amine

HRID 55359ノート

反応式

HRID 55359 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[N:9]1[C:13]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=2)=[CH:12][C:11](C(O)=O)=[N:10]1.C([N:26](CC)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.[C:48]([O-:51])(O)=[O:49].[Na+].[C:53](O)([CH3:56])([CH3:55])[CH3:54]>>[C:53]([O:51][C:48]([NH:26][C:11]1[CH:12]=[C:13]([C:14]2[CH:15]=[CH:16][C:17]([Cl:20])=[CH:18][CH:19]=2)[N:9]([C:3]2[CH:4]=[CH:5][C:6]([Cl:8])=[CH:7][C:2]=2[Cl:1])[N:10]=1)=[O:49])([CH3:56])([CH3:55])[CH3:54]

参加物

6

実験手順

3.25 g of the 1-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyrazole-3-carboxylic acid obtained according to Example 1C) and then 1.32 ml of triethylamine are added to a solution of 2.05 ml of diphenylphosphoryl azide in 40 ml of anhydrous t-butanol and the reaction mixture is refluxed under nitrogen for 12 hours. After cooling, it is treated with a saturated solution of NaHCO3 and extracted with ethyl acetate. After washing with water and then with a saturated solution of NaCl, drying over MgSO4 and evaporation of the solvents, the crude product is purified by chromatography on 70-230 mesh silica gel using CH3OH/CH2Cl2 1/99 (v/v) as the eluent to give 1.09 g of the expected product.

後処理

  1. temperaturethe reaction mixture is refluxed under nitrogen for 12 hours
  2. temperatureAfter cooling
  3. extractionextracted with ethyl acetate
  4. washAfter washing with water
  5. dry with materialwith a saturated solution of NaCl, drying over MgSO4 and evaporation of the solvents
  6. customthe crude product is purified by chromatography on 70-230 mesh silica gel

出典と根拠

ORDレコード
ord-04468ee7ec334cba8d7a8a0d96adecf8
出典データセット
uspto-grants-1997_04
特許番号
US05624941

反応ノート

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