HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Piperidone → 7.8,9,10-Tetrahydrothieno[3.2-e]pyrido[4,3-b]indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Piperidone | HCID 33721 | — |
| Reactant | (1-Benzothiophen-5-yl)hydrazinehydrochloride | HCID 20484314 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 7.8,9,10-Tetrahydrothieno[3.2-e]pyrido[4,3-b]indole | HCID 21249237 | — |
Reaction Steps
15 g of 5-hydrazinobenzothiophene hydrochloride and 15 g of 4-piperidone are boiled in 450 ml of isopropanol under a reflux condenser for 2 hours. After cooling the mixture, the precipitate which has separated out is filtered off and suspended in 2 N NaOH. A layer of methylene chloride is introduced under the suspension and the mixture is stirred; the layers are then separated and the organic phase is washed, dried and evaporated. After recrystallisation of the residue from isopropanol, 7,8,9,10-tetrahydrothieno[3,2-e]pyrido[4,3-b]indole of melting point 190° is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04410536 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-aa943656867f46beaa127ff12ce24459 |
| Source note | uspto-grants-1983_10 |