反应 #1509666

ord-862560c58b5e4274b693944763ce029e

反应方程式

CC(C)n1ncc2c(NCCc3ccc(O)cc3)nc(Cl)nc21
4-(2-(6-chloro-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino)ethyl)phenol
OB(O)c1cncc(F)c1
5-fluoropyridin-3-ylboronic acid
CC(C)n1ncc2c(NCCc3ccc(O)cc3)nc(-c3cncc(F)c3)nc21
title compound
CC(C)n1ncc2c(NCCc3ccc(O)cc3)nc(-c3cncc(F)c3)nc21
4-(2-(6-(5-fluoropyridin-3-yl)-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino)ethyl)phenol

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The crude residue was purified by reverse-phase HPLC (C18 column, eluting with ACN—H2O 0.05% TFA)

实验过程

Following the procedure of Example 15d, 4-(2-(6-chloro-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino)ethyl)phenol (b) was reacted with 5-fluoropyridin-3-ylboronic acid. The crude residue was purified by reverse-phase HPLC (C18 column, eluting with ACN—H2O 0.05% TFA) to afford the title compound as an off-white solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08927281B2uspto-grants-2015_01