反応 #607855

ord-ab7d1b55eac745b5a5aaeb4dd9213999

反応方程式

NC(=O)c1cc(Oc2cc(F)c(N)cc2F)ccn1
4-(4-amino-2,5-difluorophenoxy)picolinamide
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)Nc2cc(F)c(Oc3ccnc(C(N)=O)c3)cc2F)c(=O)n(-c2ccccc2)n1C
title compound
収率 64.0%
Cc1c(C(=O)Nc2cc(F)c(Oc3ccnc(C(N)=O)c3)cc2F)c(=O)n(-c2ccccc2)n1C
4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)-2,5-difluorophenoxy)picolinamide
収率 64.0%

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cooled to rt
  2. 2
    ろ過The solid was collected through filtration
  3. 3
    その他dried at 45° C. in vacuo overnight

実験手順

To a solution of 4-(4-amino-2,5-difluorophenoxy)picolinamide (200 mg, 0.76 mmol), and 1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylic acid (165 mg, 0.75 mmol) in DCM (10 mL) was added EDCI (175 mg, 0.93 mmol), and HOAT (26 mg, 0.15 mmol). The reaction was stirred at 45° C. for 16 hours, cooled to rt and diluted with EtOAc (20 mL). The solid was collected through filtration, dried at 45° C. in vacuo overnight to give the title compound as a white solid (230 mg, 63.7%).

出典

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