HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-6,7-dimethoxy-4-quinazolinamine → 8-[1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-3-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-6,7-dimethoxy-4-quinazolinamine | HCID 90235 | — |
| Reactant | 8-(3-Piperidinyl)-8-azaspiro[4,5]decan-7,9-dione | HCID 20556261 | — |
| Solvent | Isoamyl Alcohol | HCID 31260 | — |
| Product | 8-[1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-3-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride | HCID 20556251 | — |
Reaction Steps
The mixture of 3.75 g of 8-(3-piperidinyl)-8-azaspiro[4,5]decan-7,9-dione, 3.59 g of 4-amino-2-chloro-6,7-dimethoxyquinazoline and 100 ml of isoamyl alcohol is stirred and refluxed under nitrogen for 24 hours. It is cooled to 20°, the solids filtered off, washed with isoamyl alcohol and diethyl ether and recrystallized from the mixture of 160 ml of methanol and 110 ml of water, to yield the 8-[1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-3-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride melting at 311°-312° with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04309541 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-0dc5756a398d43c4bb2551379080d6cd |
| Source note | uspto-grants-1982_01 |