HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 21560784, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl 4-cyanopiperazine-1-carboxylate | HCID 14023627 | — |
| Reactant | HCID 21560802 | HCID 21560802 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 21560784 | HCID 21560784 | — |
Reaction Steps
A solution containing 2.62 g. (0.01 mole) of 3,4,5-trimethoxy-2-aminobenzamidine hydrochloride and 1.83 g. (0.01 mole) of 1-cyano-4-ethoxycarbonylpiperazine in 50 ml. of anhydrous ethanol is stirred at ambient temperature overnight. A 5-ml. aliquot of triethylamine is then added and the reaction mixture is heated under reflux for 12 hours. It is then worked up as described in Example XI, giving 6,7,8-trimethoxy-4-amino-2-[4-ethoxycarbonylpiperazin-1-yl]quinazoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03935213 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-8318332a755a40218e57f4a578472c46 |
| Source note | uspto-grants-1976_01 |