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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723744Generated: October 30, 2026

Lawesson's reagent → 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carbothioic acid O-ethyl ester

https://huagongshe.com/reaction/1723744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantEthyl 1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylateHCID 57467979—
SolventTolueneHCID 1140—
Product1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carbothioic acid O-ethyl esterHCID 865909945%

Reaction Steps

To a solution of ethyl 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate (0.51 g, 2 mmol) in toluene (20 mL) was added Lawesson's reagent (1.45 g, 3.6 mmol). The resulting suspension was heated to reflux under nitrogen for 24 hours. Solvent was evaporated to give the crude product, which was purified by column chromatography on silica gel eluting with MeOH-DCM (1:19) to give 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carbothioic acid O-ethyl ester (27 mg); MS (ES): 273 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485634B2
Source datasetuspto-grants-2009_02
ORD IDord-89b19eb4e4574dc2bd3cb795886e5135
Source noteuspto-grants-2009_02