HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexahydro-1,4-diazepine → (1,4-Diazepan-1-yl)(oxolan-2-yl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | 2-Furancarbonyl chloride | HCID 68242 | — |
| Reactant | (1,4-diazepan-1-yl)(furan-2-yl)methanone | HCID 12694336 | — |
| Product | (1,4-Diazepan-1-yl)(oxolan-2-yl)methanone | HCID 13100546 | — |
Reaction Steps
In the illustrated reactions, the compound of Formula II is prepared by reacting hexahydro-1,4-diazepine with furoyl chloride in an acid solution. The resultant 1-(2-furoyl)-hexahydro-1,4-diazepine is hydrogenated to produce 1-(tetrahydro-2-furoyl)-hexahydro-1,4-diazepine which is reacted with 2-chloro-4-amino-6,7-dimethoxyquinazoline in the presence of methoxy ethanol to give the compound 2-[4-(tetrahydro-2-furoyl)-hexahydro-1,4-diazepinyl-1]-4-amino-6,7-dimethoxy quinazoline. The hydrochloride salt is prepared by acidifying with hydrogen chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04044135 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-75f1392c8845479589bb0ae4645487e0 |
| Source note | uspto-grants-1977_08 |