Water → 3-Fluoro-4-(3-(2-pyridyl)-1-pyrazolyl)phenyl carbamic acid benzyl ester

HRID 1844505ノート

反応式

HRID 1844505 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[N:9]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=2)=[N:10]1)[NH2:5].C(=O)([O-])[O-].[K+].[K+].[CH:26]1[CH:31]=[CH:30][C:29]([CH2:32][O:33][C:34](Cl)=[O:35])=[CH:28][CH:27]=1.O>ClCCl>[CH2:32]([O:33][C:34](=[O:35])[NH:5][C:4]1[CH:6]=[CH:7][C:8]([N:9]2[CH:13]=[CH:12][C:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=3)=[N:10]2)=[C:2]([F:1])[CH:3]=1)[C:29]1[CH:30]=[CH:31][CH:26]=[CH:27][CH:28]=1

参加物

6

反応物 4

HCID 962WaterHCID 10387Benzyl chloroformateHCID 11430Potassium CarbonateHCID 867193713-fluoro-4-(3-(pyridin-2-yl)-1H-pyrazol-1-yl)aniline

生成物 1

HCID 867193723-Fluoro-4-(3-(2-pyridyl)-1-pyrazolyl)phenyl carbamic acid benzyl ester収率 81.5%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

The above-described product 19a (1 g, 3.9 mmol) was dissolved in dichloromethane (4 mL), and then anhydrous potassium carbonate (0.6 g) was added thereto. Then, Cbz-Cl (1.863 g, 1.537 mL) was slowly dropped, at a rate of 1-2 drops per second, into the mixture maintained in an ice-salt bath. The resultant mixture was reacted for 4 hours at room temperature. After completion of the reaction, water was added into the reaction mixture, followed by extraction with ethyl acetate. The combined ethyl acetate phase was evaporated in vacuum to get a crude product, which was recrystallized with acetone to afford the product 20a (1.235 g) as a white solid, with a yield of 80.8%.

後処理

  1. temperaturemaintained in an ice-salt bath
  2. additionwas added into the reaction mixture
  3. extractionfollowed by extraction with ethyl acetate
  4. customThe combined ethyl acetate phase was evaporated in vacuum
  5. customto get a crude product, which
  6. customwas recrystallized with acetone

出典と根拠

ORDレコード
ord-da71513000f3410ca597590bcbc90d6c
出典データセット
uspto-grants-2015_02
特許番号
US08946436B2

反応ノート

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