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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Chlorothiophene | HCID 7299 | — |
| Reactant | Methyl 7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate | HCID 22328963 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 7-bromo-1-(2-thienylcarbonyl)-2,3-dihydro-1-benzazepine-4-carboxylate | HCID 22329012 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936602B1 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-1ffd5f06a8b64fbd800d5841614c67fb |
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| Source note | uspto-grants-2005_08 |
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