HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinazoline | HCID 2769364 | — |
| Reactant | 1,4-Dioxa-8-azaspiro[4.5]decane--hydrogen chloride (1/1) | HCID 16218795 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinone | HCID 14738823 | 98% |
Reaction Steps
4-Chloro-6,7-dimethoxyquinazoline (30 g), 4-piperidone ethylene ketal hydrochloride (25 g), triethylamine (35 g) and ethanol (250 ml.) were refluxed together for 3 hours. Aqueous sodium carbonate was added followed by extraction with chloroform after which the chloroform extract was dried and evaporated in vacuo to give an oil. The oil was redissolved in aqueous hydrochloric acid (1.5N, 200 ml.) and refluxed for 2 hours followed by cooling, basification (Na2CO3 10% soln) and extraction into chlororform. Evaporation of the dried chloroform extract gave 4-(4-oxo-piperidino)-6,7-dimethoxyquinazoline (37.6 g) m.p. 176°-8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04001422 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-074f683bb77c4dde8950488fef0c78a2 |
| Source note | uspto-grants-1977_01 |