反应 #1509671

ord-a9272923e6084e0ebb3fcfd41c10233b

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 preparative HPLC

实验过程

Following the procedure of Example 15d, (R)-4-(2-(2-chloro-9-(tetrahydrofuran-3-yl)-9H-purin-6-ylamino)ethyl)phenol (c) was reacted with benzo[b]thiophen-3-ylboronic acid (22.3 mg, 0.125 mmol). The crude residue was purified by reverse-phase preparative HPLC 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