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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736107Generated: October 30, 2026

4-Fluorobenzoyl chloride → 3-(4-Fluorobenzoyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/736107

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantEthyl 1,2,3,4,5,6-hexahydroazepino[4,5-b]indole-5-carboxylateHCID 57559105—
SolventDichloromethaneHCID 6344—
Product3-(4-Fluorobenzoyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole-5-carboxylic acid ethyl esterHCID 66640105—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of ethyl 1,2,3,4,5,6-hexahydroazepino[4,5-b]indole-5-carboxylate (0.46 g, 1.8 mmol) in DCM (6 mL) was added 4-fluorobenzoyl chloride (0.26 mL, 1.2 equiv) and TEA (0.38 mL, 1.5 equiv) and the mixture was stirred for 1 hour at 20° C. Evaporation of solvent gave a crude product, which was purified by column chromatography on silica gel eluting with MeOH-DCM (1:9) to afford 3-(4-fluorobenzoyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester; (543 mg, 80%) MS (ES): 381 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595311B2
Source datasetuspto-grants-2009_09
ORD IDord-3ce6d4f00d6b40f78613f5e208b7279d
Source noteuspto-grants-2009_09