反应 #1509595

ord-c0508a5dcc9945de9147310e74c962ad

反应方程式

Clc1cc(-c2cnn(C3CCCCO3)c2)ccn1
2-Chloro-4-[1-(tetrahydro-pyran-2-yl)-1H-pyrazol-4-yl]-pyridine
Cc1noc(C)c1Br
4-bromo-3,5-dimethylisoxazole
Cc1noc(C)c1-c1ccnc(Cl)c1
title compound
Cc1noc(C)c1-c1ccnc(Cl)c1
2-Chloro-4-(3,5-dimethyl-isoxazol-4-yl)-pyridine

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他HPLC (Rt)=0.81 min (method N)

实验过程

The title compound was prepared from 4-bromo-3,5-dimethylisoxazole generally according to the synthetic procedure described for 2-Chloro-4-[1-(tetrahydro-pyran-2-yl)-1H-pyrazol-4-yl]-pyridine. HPLC (Rt)=0.81 min (method N)

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE045323E1uspto-grants-2015_01