HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → N-(3,4-dihydro-2-methyl-4-oxoquinazolin-6-ylmethyl) N-ethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 6-(Bromomethyl)-2-methyl-4(1H)-quinazolinone | HCID 135442581 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(3,4-dihydro-2-methyl-4-oxoquinazolin-6-ylmethyl) N-ethylamine | HCID 136093134 | — |
Reaction Steps
A mixture of 6-bromomethyl-3,4-dihydro-2-methylquinazolin-4-one (prepared as described in Example 3; 10 g), anhydrous ethylamine (7.9 ml) and acetonitrile (250 ml) was stirred rapidly at laboratory temperature for 4 hours. The mixture was evaporated to dryness, the residue was dissolved in water, filtered and the filtrate was evaporated. The residue was triturated in acetone to give N-(3,4-dihydro-2-methyl-4-oxoquinazolin-6-ylmethyl)-N-ethylamine, as its hydrobromide salt (8.5 g), m.p. >260° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05081124 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-e08ed2c721ad4085b17d702933a4224b |
| Source note | uspto-grants-1992_01 |