HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-(4-Cyanopiperazin-1-yl)-4-amino-6,7-dimethoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Bromo-6,7-dimethoxyquinazolin-4-amine | HCID 20320512 | — |
| Reactant | Piperazine-1-carbonitrile | HCID 22633091 | — |
| Product | 2-(4-Cyanopiperazin-1-yl)-4-amino-6,7-dimethoxyquinazoline | HCID 21393366 | — |
Reaction Steps
In a flask fitted with stirrer, thermometer, and drying tube is placed 100 ml. of chloroform, 12.0 g. (0.05 mole) of 4-amino-2-bromo-6,7-dimethoxyquinazoline (prepared by the method of U.S. Pat. No. 3,511,836) and 5.8 g. (0.052 mole) of 1-cyanopiperazine. The mixture is maintained at 50° C. for 24 hours after which 2N potassium hydroxide solution is added at room temperature to adjust to pH 9.5. The organic layer is separated and the aqueous phase extracted again with chloroform and the combined extracts are evaporated to dryness to obtain 2-(4-cyanopiperazin-1-yl)-4-amino-6,7-dimethoxyquinazoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04062844 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-610d6ab3dd524579bd5a158c02a818e0 |
| Source note | uspto-grants-1977_12 |