反応 #957594

ord-15fa2c60040d43cb944194a1bd3c5742

反応方程式

Nc1ccc(Oc2ccnc(N)c2)cc1
4-(4-aminophenoxy)pyridin-2-amine
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(Oc3ccnc(N)c3)cc2)c(=O)n(-c2ccccc2)n1C
title compound
収率 53.0%
Cc1c(C(=O)Nc2ccc(Oc3ccnc(N)c3)cc2)c(=O)n(-c2ccccc2)n1C
N-(4-((2-aminopyridin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide
収率 53.0%

溶媒

反応条件

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

後処理

  1. 1
    その他quenched with water (20 mL)
  2. 2
    その他The organic phase was separated
  3. 3
    濃縮concentrated in vacuo
  4. 4
    その他The residue was purified by a silica gel column chromatography (DCM/CH3OH (v/v)=20/1)

実験手順

To a mixture of 4-(4-aminophenoxy)pyridin-2-amine (101 mg, 0.5 mmol) and 1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylic acid (118 mg, 0.51 mmol) in DCM (5 mL) was added EDCI (115 mg, 0.6 mmol) and HOAT (13.6 mg, 0.1 mmol). The reaction was stirred at 45° C. for 3 hours, and then quenched with water (20 mL). The organic phase was separated and concentrated in vacuo. The residue was purified by a silica gel column chromatography (DCM/CH3OH (v/v)=20/1) to give the title compound as a light grey solid (110 mg, 49.2%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08969388B1uspto-grants-2015_03