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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265436Generated: October 27, 2026

4-(((4-Methoxyphenyl)amino)methyl)-N,N-dimethylaniline → N-[(4-dimethylaminophenyl)methyl]-7-fluoro-N-(4-methoxyphenyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide

https://huagongshe.com/reaction/2265436

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(((4-Methoxyphenyl)amino)methyl)-N,N-dimethylanilineHCID 855075—
Reactant7-Fluoro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acidHCID 17854522—
ProductN-[(4-dimethylaminophenyl)methyl]-7-fluoro-N-(4-methoxyphenyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamideHCID 59597237—

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-methoxyphenyl)amine (0.54 g) as starting materials, N-[(4-dimethylaminophenyl)methyl]-7-fluoro-N-(4-methoxyphenyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide 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-methoxyphenyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide hydrochloride ½ hydrate (0.52 g). melting point: 125.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855297B2
Source datasetuspto-grants-2010_12
ORD IDord-76d4d77b3bcb41bfb3dcd8d7c358e057
Source noteuspto-grants-2010_12