HRID218550

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11208318

1,2,3,4-Tetrahydro-5-(phenylmethoxy)-1-naphthalenecarboxylic acid

C18H18O3

HCID17854288

6-(Propan-2-yl)pyridin-3-amine

C8H12N2

PRODUCTS

生成物

结构：CC(C)c1ccc(NC(=O)C2CCCc3c(OCc4ccccc4)cccc32)cn1

HCID17854215

未命名化合物

收率 73.5%

PROCEDURE

实验过程

By the reaction and treatment in the same manner as in Preparation Example 11 using 5-benzyloxy-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid (1.06 g) and 5-amino-2-isopropylpyridine (0.50 g) as starting materials, 5-benzyloxy-N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide (1.08 g) was obtained. melting point: 157.4° C.

WORKUP

后处理

customBy the reaction and treatment in the same manner