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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218666Generated: October 25, 2026

7-Fluoro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid → N-[(4-dimethylaminophenyl)methyl]-7-fluoro-N-(4-isopropylphenyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide

https://huagongshe.com/reaction/218666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Fluoro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acidHCID 17854522—
ReactantN-(4-(Dimethylamino)benzyl)-4-isopropylbenzenamineHCID 21957887—
ProductN-[(4-dimethylaminophenyl)methyl]-7-fluoro-N-(4-isopropylphenyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamideHCID 1667966390.6%

Reaction Steps

By the reaction and treatment in the same manner as in Example 12 using 7-fluoro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid (0.41 g) and [(4-dimethylaminophenyl)methyl](4-isopropylphenyl)amine (0.57 g) as starting materials, N-[(4-dimethylaminophenyl)methyl]-7-fluoro-N-(4-isopropylphenyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide (0.85 g) was obtained. This compound was dissolved in ethyl acetate, and 4 mol/L-HCl/dioxane was added. The precipitated solid was collected by filtration to give N-[(4-dimethylaminophenyl)methyl]-7-fluoro-N-(4-isopropylphenyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide hydrochloride (0.85 g). melting point: 165.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198454B2
Source datasetuspto-grants-2012_06
ORD IDord-99aaf2bbfef24606b8f67bb1e34fb968
Source noteuspto-grants-2012_06