HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → 4H-pyrimido[1,2-c]quinazoline-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,2-Dimethyl-5-[(4-quinazolinyl)amino]methylene-1,3-dioxane-4,6-dione | HCID 13060518 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | 4H-pyrimido[1,2-c]quinazoline-4-one | HCID 13060570 | 69.4% |
Reaction Steps
A mixture of 2,2-dimethyl-5-[(4-quinazolinyl)amino]methylene-1,3-dioxane-4,6-dione (3.5 g) in diphenylether (15 ml) was stirred for 10 minutes at 250°-260° C. and then cooled to ambient temperature. To the reaction mixture was added hexane and allowed to to stand at ambient temperature to give crystals, which were separated by filtration and washed with hexane to give crude crystals (3 g). The crude crystals were subjected to a column chromatography using silica gel (developing solvent: a mixture of ethyl acetate and hexane (3:7)). The eluate was concentrated under reduced pressure to give crystals, which were recrystallized from chloroform and hexane to give 4H-pyrimido[1,2-c]quinazoline-4-one (1.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04377580 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-da56535d6c40405bb8c1363e0f6181e7 |
| Source note | uspto-grants-1983_03 |