反应 #1881000

ord-ce9315157eec419f96c9f7f424271881

反应方程式

CCCn1c(=O)[nH]c(=O)c2[nH]c(C34CCC(C=CC(=O)OC)(CC3)CC4)nc21
3-[4-(2,6-Dioxo-3-propyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]oct-1-yl]-acrylic acid methyl ester
CCCn1c(=O)[nH]c(=O)c2[nH]c(C34CCC(CCC(=O)OC)(CC3)CC4)nc21
desired product
收率 92.8%
CCCn1c(=O)[nH]c(=O)c2[nH]c(C34CCC(CCC(=O)OC)(CC3)CC4)nc21
3-[4-(2,6-Dioxo-3-propyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]oct-1-yl]-propionic acid methyl ester
收率 92.8%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他the resulting reaction mixture
  2. 2
    过滤The reaction mixture was filtered through Celite
  3. 3
    浓缩the filtrate was concentrated under reduced pressure

实验过程

3-[4-(2,6-Dioxo-3-propyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]oct-1-yl]-acrylic acid methyl ester (300 mg) was dissolved in 20 mL of THF. 10% Pd on C (25 mg) was added and the resulting reaction mixture was hydrogenated under 50 psi of H2 at rt for 6 h. The reaction mixture was filtered through Celite and the filtrate was concentrated under reduced pressure to afford 280 mg of the desired product.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07022686B2uspto-grants-2006_04