HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lawesson's reagent → 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carbothioic acid O-ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | Ethyl 1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylate | HCID 57467979 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carbothioic acid O-ethyl ester | HCID 86590994 | 5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07485634B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-89b19eb4e4574dc2bd3cb795886e5135 |
| Source note | uspto-grants-2009_02 |