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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265319Generated: October 31, 2026

5-Benzyloxy-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid → 5-benzyloxy-N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide

https://huagongshe.com/reaction/2265319

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzyloxy-1,2,3,4-tetrahydronaphthalene-1-carboxylic acidHCID 11208318—
Reactant6-(Propan-2-yl)pyridin-3-amineHCID 17854288—
Product5-benzyloxy-N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamideHCID 1785421573.5%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855297B2
Source datasetuspto-grants-2010_12
ORD IDord-103abdd2ad6041d99665d88106d9e9c8
Source noteuspto-grants-2010_12