反応 #607864

ord-274766ff36894456969b769d60e37f9c

反応方程式

Nc1ccc(O)c(F)c1
4-amino-2-fluorophenol
Cc1c(C(=O)O)c(=O)n(-c2ccccc2)n1C
1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylic acid
CCN=C=NCCCN(C)C
EDCI
On1nnc2cccnc21
HOAT
Cc1c(C(=O)Nc2ccc(O)c(F)c2)c(=O)n(-c2ccccc2)n1C
title compound
収率 93.4%
Cc1c(C(=O)Nc2ccc(O)c(F)c2)c(=O)n(-c2ccccc2)n1C
N-(3-fluoro-4-hydroxyphenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide
収率 93.4%

溶媒

反応条件

温度
45°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cool to rt
  2. 2
    その他quenched with H2O (10 mL)
  3. 3
    workup.STIRRINGstirred for another 4 hours
  4. 4
    その他The solid was obtained by filtration
  5. 5
    洗浄washed with DCM (20 mL×3)
  6. 6
    その他dried at 60° C. in vacuo for 12 hours

実験手順

To a suspension of 4-amino-2-fluorophenol (2.54 g, 20 mmol) and 1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylic acid (4.74 g, 20.4 mmol) in DCM (60 mL) were added EDCI (4.6 g, 24 mmol) and HOAT (0.54 g, 4 mmol). The reaction was stirred at 45° C. for 12 hours, then cool to rt, quenched with H2O (10 mL), and stirred for another 4 hours. The solid was obtained by filtration and washed with DCM (20 mL×3), then dried at 60° C. in vacuo for 12 hours to give the title compound as a pale yellow solid (6.37 g, 93.4%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09326975B2uspto-grants-2016_05