Ammonium Chloride → (-)-2-(1-ethyl-1H-pyrazol-4-yl)-9-hydroxy-9-trifluoromethyl-9H-fluorene-4-carboxamide

HRID 1799019ノート

反応式

HRID 1799019 の反応式
C(N1[CH:7]=[C:6]([C:8]2[CH:20]=[C:19]([C:21](O)=O)[C:18]3[C:17]4[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=4)[C:11]([OH:28])([C:24]([F:27])([F:26])[F:25])[C:10]=3[CH:9]=2)[CH:5]=[N:4]1)C.Cl.CN(C)[CH2:32][CH2:33]CN=C=NCC.[OH2:41].O[N:43]1C2C=CC=CC=2N=N1.[Cl-].[NH4+:53]>C(OCC)(=O)C.C(N(CC)CC)C.CN(C)C=O>[CH2:32]([N:53]1[CH:7]=[C:6]([C:8]2[CH:20]=[C:19]([C:21]([NH2:43])=[O:41])[C:18]3[C:17]4[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=4)[C:11]([OH:28])([C:24]([F:25])([F:27])[F:26])[C:10]=3[CH:9]=2)[CH:5]=[N:4]1)[CH3:33]

参加物

8

実験手順

To a mixture of an optically active form (0.051 g) of 2-(1-ethyl-1H-pyrazol-4-yl)-9-hydroxy-9-trifluoromethyl-9H-fluorene-4-carboxylic acid, 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.038 g), 1-hydroxybenzotriazole hydrate (0.030 g), ammonium chloride (0.022 g) and dimethylformamide (1 ml) was added triethylamine (0.055 ml), and the mixture was stirred at room temperature overnight. To the reaction mixture was added ethyl acetate (10 ml), and the organic layer was successively washed once with hydrochloric acid, once with water, twice with saturated aqueous sodium hydrogen carbonate, 3 times with water and once with saturated brine. The organic layer was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure to give the title compound (0.043 g, 85%).

後処理

  1. washthe organic layer was successively washed once with hydrochloric acid, once with water, twice with saturated aqueous sodium hydrogen carbonate, 3 times with water and once with saturated brine
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-d40adeba5ec84be1a01acbbb6d994a33
出典データセット
uspto-grants-2013_01
特許番号
US08343994B2

反応ノート

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