HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 21412364, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2-Chloroquinazolin-4-amine | HCID 252879 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21412364 | HCID 21412364 | — |
Reaction Steps
A mixture of 5 g of 2-chloro-4-aminoquinazoline, 5 ml of 4-methylpiperazine, and 10 ml of ethanol was heated at reflux overnight. The reaction mixture was diluted with 200 ml of water, made alkaline with 15 ml of 50 percent sodium hydroxide solution, and extracted with 500 ml of ether. The ether extract was washed with water, dried over anhydrous sodium sulfate, and filtered. The ether was removed by evaporation. The residue was dissolved in 500 ml of dry ether and treated with excess hydrogen chloride. Filtration afforded 1.5 g of 2-(4-methylpiperazinyl)-4-aminoquinazoline hydrochloride; m.p. 333°-334° with decomposition. The following analytical data were obtained:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04048312 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-1dbbccfc00a44dbdaedfa626f1ec6aca |
| Source note | uspto-grants-1977_09 |