Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587023Generated: October 26, 2026

Water → Methyl 7-bromo-1-(2-thienylcarbonyl)-2,3-dihydro-1-benzazepine-4-carboxylate

https://huagongshe.com/reaction/587023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant2-ChlorothiopheneHCID 7299—
ReactantMethyl 7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylateHCID 22328963—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 7-bromo-1-(2-thienylcarbonyl)-2,3-dihydro-1-benzazepine-4-carboxylateHCID 22329012—

Reaction Conditions

Temperature78 °C

Reaction Steps

To a solution of methyl 7-bromo-2,3-dihydro-1-benzazepine-4-carboxylate (200 mg) and pyridine (123 mg) in tetrahydrofuran (10 ml) was added 2-thienyl chloride (208 mg) at 0° C., and the mixture was heated at 78° C. overnight. After allowing to cool, to the mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried with magnesium sulfate. The solvent was evaporated, which was recrystallized from hexane-ethyl acetate to give methyl 7-bromo-1-(2-thienylcarbonyl)-2,3-dihydro-1-benzazepine-4-carboxylate (236 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-1ffd5f06a8b64fbd800d5841614c67fb
Source noteuspto-grants-2005_08