Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265466Generated: November 1, 2026

7-Methoxy-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid → n-(4-Bromophenyl)-n-[(4-dimethylaminophenyl)methyl]-7-methoxy-1,2,3,4-tetrahydronaphthalene-1-carboxamide hydrochloride

https://huagongshe.com/reaction/2265466

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Methoxy-1,2,3,4-tetrahydronaphthalene-1-carboxylic acidHCID 13277484—
Reactant4-[(4-Bromoanilino)methyl]-N,N-dimethylanilineHCID 15174101—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
SolventEthyl AcetateHCID 8857—
Productn-(4-Bromophenyl)-n-[(4-dimethylaminophenyl)methyl]-7-methoxy-1,2,3,4-tetrahydronaphthalene-1-carboxamide hydrochlorideHCID 67183700—

Reaction Steps

7-Methoxy-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid (0.47 g) and (4-bromophenyl)[(4-dimethylaminophenyl)methyl]-amine (0.70 g) as starting materials were reacted and treated in the same manner as in Example 12. The obtained solid was dissolved in ethyl acetate (4 mL). Thereto was added 4 mol/L-HCl/ethyl acetate (0.35 mL), and the precipitated solid was collected by filtration to give N-(4-bromophenyl)-N-[(4-dimethylaminophenyl)methyl]-7-methoxy-1,2,3,4-tetrahydronaphthalene-1-carboxamide hydrochloride (0.65 g). melting point: 104-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855297B2
Source datasetuspto-grants-2010_12
ORD IDord-533f5ec7ffea4acdbeab686766a730b0
Source noteuspto-grants-2010_12