HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(alpha-Hydroxymethyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18796707 | HCID 18796707 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(alpha-Hydroxymethyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline | HCID 18796788 | 16.8% |
Reaction Steps
10 ml of ethanol and 197 mg of sodium borohydride were added to 200 mg of 4-(α-ethoxycarbonyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline. The obtained mixture was refluxed for 30 minutes, followed by the addition of 5 ml of water. The obtained mixture was concentrated under a reduced pressure, followed by the addition of 10 ml of water. The crystal thus precipitated was recovered by filtration. Thus, 30 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-f56050e9092f4fa6b642805d6aa1c89d |
| Source note | uspto-grants-1998_09 |