HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-6,7-dimethoxy-4-quinazolinamine → HCID 13723660, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-6,7-dimethoxy-4-quinazolinamine | HCID 90235 | — |
| Reactant | (2,3-Dihydro-1,4-benzodioxin-2-yl)(hexahydro-1H-1,4-diazepin-1-yl)methanone | HCID 13723686 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 13723660 | HCID 13723660 | 17.2% |
Reaction Steps
4-Amino-2-chloro-6,7-dimethoxyquinazoline (1.58 g.) and N-(1,4-benzodioxan-2-carbonyl)homopiperazine (2.0 g.) were heated under reflux in n-butanol (114 ml.) for 60 hours. The mixture was then cooled, butanol removed in vacuo and the solid residue triturated with ether, taken up in hot methanol, filtered and cooled. The solid product was collected, then the residual solution was evaporated in vacuo and the residue taken up in hot isopropanol, cooled, filtered, then re-evaporated in vacuo. The residue was combined with the original solid product, treated with cold methanol, and recrystallized from ethanol to give 4-amino-2-[4-(1,4-benzodioxan-2-carbonyl)homopiperazin-1-yl]-6,7-dimethoxyquinazoline hydrochloride (0.57 g.), m.p. 250°-251° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04188390 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-7e753f9957b1465d8a0e64281c8e7269 |
| Source note | uspto-grants-1980_02 |