HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(alpha-Carboxy-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18796707 | HCID 18796707 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(alpha-Carboxy-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline | HCID 18796662 | 48.5% |
Reaction Steps
10 ml of ethanol, 5 ml of water and 20 mg of sodium hydroxide were added to 100 mg of 4-(α-ethoxycarbonyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline. The obtained mixture was refluxed for 10 minutes and concentrated under a reduced pressure, followed by the addition of 20 ml of water. The obtained mixture was neutralized with 1N hydrochloric acid. The crystal thus precipitated was recovered by filtration. Thus, 45 mg of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05801180 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-ed5dbe43088044749e5826e13887a019 |
| Source note | uspto-grants-1998_09 |