HRID1272317

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：COc1ccc(N2CCN(c3c(C)c(C)c4c(c3C)C(O)(c3ccc(OC)cc3)C(C)(C)O4)CC2)cc1

HCID58847352

未命名化合物

PRODUCTS

生成物

结构：COc1ccc(C2c3c(C)c(N4CCN(c5ccc(OC)cc5)CC4)c(C)c(C)c3OC2(C)C)cc1

HCID18456073

未命名化合物

收率 88%

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID702

Ethanol

C2H6O

PROCEDURE

实验过程

Using 3-(4-methoxyphenyl)-5-(4-(4-methoxyphenyl)piperazin-1-yl)-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-3-ol obtained in Example 66, the title compound was synthesized in the same manner as in Example 46. Yield 88%. mp. 205–207° C. (ethanol).