HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-6,7-dimethoxy-4-quinazolinamine → HCID 20220996, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-6,7-dimethoxy-4-quinazolinamine | HCID 90235 | — |
| Reactant | 5,5-Dimethyl-3-piperazin-1-yl-cyclohex-2-enone | HCID 648131 | — |
| Solvent | Isoamyl Alcohol | HCID 31260 | — |
| Product | HCID 13520910 | HCID 13520910 | 78% |
| Product | HCID 20220996 | HCID 20220996 | 204.6% |
Reaction Steps
A mixture of 4.8 g (0.02 mol) of 2-chloro-4-amino-6,7-dimethoxyquinazoline, 4.6 g (0.022 mol) of (3-oxo-5,5-dimethyl-1-cyclohexen-1-yl)-piperazine and 80 ml of isoamyl alcohol is boiled under reflux for 3 hours, with stirring. During the reaction time, the monohydrochloride precipitates. The mixture is left to stand overnight and the crystals are filtered off with suction. After washing with 40 ml of isoamyl alcohol and twice with in each case 40 ml of absolute acetone and 40 ml of absolute ether and drying, 7.1 g of the hydrochloride of 1-(4-amino-6,7-dimethoxyquinazolin-2-yl)-4-(3-oxo-5,5-dimethyl-1-cyclohexen-1-yl)-piperazine (78% yield) of melting point 267°-268° C. (decomposition) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04639453 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-1e60c489c4ba42d28fff569f6bbcc569 |
| Source note | uspto-grants-1987_01 |