Triethylamine → N-[4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)benzyl]-4-chloro-3-ethyl-1-methyl-5-pyrazolecarboxamide

HRID 2248378

反応式

HRID 2248378 の反応式
C(OCC)(=O)C.[Cl:7][C:8]1[C:9]([O:18][C:19]2[CH:26]=[CH:25][C:22]([CH2:23][NH2:24])=[CH:21][CH:20]=2)=[N:10][CH:11]=[C:12]([C:14]([F:17])([F:16])[F:15])[CH:13]=1.C(N(CC)CC)C.CC1C=CC(OC2C=CC(CN[C:46]([C:48]3[N:52]([CH3:53])[N:51]=[C:50]([CH2:54][CH3:55])[C:49]=3[Cl:56])=[O:47])=CC=2)=CC=1>O>[Cl:7][C:8]1[C:9]([O:18][C:19]2[CH:26]=[CH:25][C:22]([CH2:23][NH:24][C:46]([C:48]3[N:52]([CH3:53])[N:51]=[C:50]([CH2:54][CH3:55])[C:49]=3[Cl:56])=[O:47])=[CH:21][CH:20]=2)=[N:10][CH:11]=[C:12]([C:14]([F:17])([F:15])[F:16])[CH:13]=1

参加物

6

実験手順

Into 50 ml solution of ethyl acetate containing 2.49 g of 4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)benzylamine and 1.21 g of triethylamine, was dropped 2.07 g of 4-chloro-3-ethyl-1-methyl-5-pyrazolecarboxylic acid chloride synthesized in Example 2. After the completion of dropping, the mixture was stirred for 1 hour, poured into iced water and then extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous solution of sodium carbonate, water and a saturated aqueous solution of sodium chloride. After drying over anhydrous sodium sulfate, the solution was concentrated under a reduced pressure. The residue was purified on silica gel column chromatography to obtain 3.35 g of the titled compound (No. 75) shown in Table 1.

後処理

  1. extractionextracted with ethyl acetate
  2. washThe ethyl acetate layer was washed with an aqueous solution of sodium carbonate, water
  3. dry with materialAfter drying over anhydrous sodium sulfate
  4. concentrationthe solution was concentrated under a reduced pressure
  5. customThe residue was purified on silica gel column chromatography

出典と根拠

ORDレコード
ord-d3455af18c8646cb817ae64a32cf5282
出典データセット
uspto-grants-1991_08
特許番号
US05039693

関連ノート

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