HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 2-Piperazino-6,7-dimethoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-Chloro-6,7-dimethoxyquinazoline | HCID 1818144 | — |
| Solvent | Isoamyl Alcohol | HCID 31260 | — |
| Product | 2-Piperazino-6,7-dimethoxyquinazoline | HCID 13784185 | 91% |
Reaction Steps
Refluxed for 2 hours in isoamyl alcohol (15 ml) were 0.63 g of 2-chloro-6,7-dimethoxyquinazoline (synthesized by the method described in Japanese Patent Laid-Open No. 36390/1972) and 0.72 g of anhydrous piperazine. Isoamyl alcohol was thereafter distilled off under reduced pressure, followed by extraction with 2N--NaOH and chloroform. The chloroform layer was washed with saturated saline and then dried with anhydrous magnesium sulfate. Chloroform was distilled off under reduced pressure to obtain 0.7 g of the intended product (yield: 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04734418 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-021aededadf048898074c8fd46bc7614 |
| Source note | uspto-grants-1988_03 |