反应 #470418

ord-61bfacac83a94dfc9e71fe3181af57f4

反应方程式

COc1ccc(C2=Cc3ccc(O)c(C)c3OC2)cc1OC
7-Hydroxy-3′,4′-dimethoxy-8-methylisoflav-3-ene
CCO
ethanol
NCc1ccccc1
Benzylamine
C=O
formaldehyde
COc1ccc(C2=Cc3cc4c(c(C)c3OC2)OCN(Cc2ccccc2)C4)cc1OC
title compound
收率 15.0%
COc1ccc(C2=Cc3cc4c(c(C)c3OC2)OCN(Cc2ccccc2)C4)cc1OC
3-Benzyl-7-(3,4-dimethoxyphenyl)-10-methyl-2,3,4,8-tetrahydro-chromeno[6,7-e][1,3]oxazine
收率 15.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The precipitate was collected

实验过程

7-Hydroxy-3′,4′-dimethoxy-8-methylisoflav-3-ene (155 mg, 0.52 mmol) was dissolved in ethanol (2.5 ml). Benzylamine (0.07 ml, 023 mmol) was added followed by formaldehyde solution (0.6 ml, 8.06 mmol, 37% wt.). The reaction was stirred at room temperature for 2 days. The precipitate was collected to afford the title compound (33 mg, 15%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08367659B2uspto-grants-2013_02