反应 #569500

ord-7e89f14f87f54e839d755c5beb2b104a

反应方程式

OCCn1c2c(c3c(N4CCCC4)nc(N4CCCC4)nc31)CCCC2
9-(2-hydroxyethyl)-2,4-di-1-pyrrolidinyl-5,6,7,8-tetrahydro-9H-pyrimido[4,5-b]indole
OCCn1c2c(c3c(N4CCCC4)nc(N4CCCC4)nc31)CCCC2
9-(2-Hydroxyethyl)-2,4-di- 1-pyrrolidinyl-5,6,7,8-tetrahydro-9H-pyrimido[4,5-b]indole
OCCn1c2ccccc2c2c(N3CCCC3)nc(N3CCCC3)nc21
title compound
OCCn1c2ccccc2c2c(N3CCCC3)nc(N3CCCC3)nc21
9-(2-Hydroxyethyl)-2,4-di-1-pyrrolidinyl-9H-pyrimido[4,5-b]indole

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度is heated
  2. 2
    温度at reflux for 3 hr
  3. 3
    温度The mixture is cooled to 20°-25°
  4. 4
    过滤filtered through diatomaceous earth
  5. 5
    其他Removal of the solvent from the filtrate

实验过程

A mixture of 9-(2-hydroxyethyl)-2,4-di-1-pyrrolidinyl-5,6,7,8-tetrahydro-9H-pyrimido[4,5-b]indole (VII, EXAMPLE2, 5.14 g) and palladium on carbon (10%, 1.4 g) in decalin (250 mL) is heated at reflux for 3 hr. The mixture is cooled to 20°-25°, diluted with methylene chloride (250 mL) and filtered through diatomaceous earth. Removal of the solvent from the filtrate, followed by chromatography (silica gel, 1% methanol/chloroform) of the resulting residue gives the title compound, mp=110°-111; MS (m/z) 351, 323, 307, 296 and 279; NMR (CDCl3) 7.89, 7.23, 7.13, 6.97, 4.38, 4.05, 3.92, 3.62 and 2.0-1.9 δ.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05795986uspto-grants-1998_08