反応 #607860

ord-1619e4cb056440a19f65efca89f1c326

反応方程式

NC(=O)c1cc(Oc2ccc(N)nc2)ccn1
4-((6-aminopyridin-3-yl)oxy)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)Nc2ccc(Oc3ccnc(C(N)=O)c3)cn2)c(=O)n(-c2ccccc2)n1C
title compound
収率 25.0%
Cc1c(C(=O)Nc2ccc(Oc3ccnc(C(N)=O)c3)cn2)c(=O)n(-c2ccccc2)n1C
4-((6-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)pyridin-3-yl)oxy)picolinamide
収率 25.0%

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
    濃縮The organic phase was concentrated in vacuo
  3. 3
    その他the residue was purified by a silica gel column chromatography (DCM/CH3OH (v/v)=40/1)

実験手順

To a suspension of 4-((6-aminopyridin-3-yl)oxy)picolinamide (230 mg, 1 mmol) and 1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylic acid (237 mg, 1.02 mmol) in DCM (5 mL) was added EDCI (230 mg, 1.2 mmol) and HOAT (27 mg, 0.2 mmol). The reaction was stirred at 45° C. for 28 hours, then cooled to rt and diluted with water (10 mL) and DCM (20 mL). The organic phase was concentrated in vacuo and the residue was purified by a silica gel column chromatography (DCM/CH3OH (v/v)=40/1) to give the title compound as a light grey solid (111 mg, 25%).

出典

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