反应 #1509673

ord-c42f18ead6df46f1b33c99c73b21dcf7

反应方程式

COC(=O)C(C)n1cnc2c(Cl)nc(Cl)nc21
methyl 2-(2,6-dichloro-9H-purin-9-yl)propanoate
NCCc1c[nH]c2ccccc12
tryptamine
COC(=O)C(C)n1cnc2c(NCCc3c[nH]c4ccccc34)nc(Cl)nc21
title compound
COC(=O)C(C)n1cnc2c(NCCc3c[nH]c4ccccc34)nc(Cl)nc21
methyl 2-(6-(2-(1H-indol-3-yl)ethylamino)-2-chloro-9H-purin-9-yl)propanoate

反应条件

温度
85°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The reaction mixture was cooled to room temperature
  2. 2
    浓缩concentrated
  3. 3
    其他The residue was purified by silica gel chromatography (10 to 80% ethyl acetate in hexane eluant)

实验过程

A mixture of methyl 2-(2,6-dichloro-9H-purin-9-yl)propanoate (b) (600 mg, 2.2 mmol), tryptamine (420 mg, 2.6 mmol) and 2-propanol (30 mL) was heated at 85° C. in a sealed tube for 16 h. The reaction mixture was cooled to room temperature and concentrated. The residue was purified by silica gel chromatography (10 to 80% ethyl acetate in hexane eluant) to afford the title compound as a white solid. MS m/z 360.1 (M+1).

来源

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