HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 22137667, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | HCID 4353710 | HCID 4353710 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22137667 | HCID 22137667 | — |
Reaction Steps
2-Ethyl-3-benzyl-quinazolin-4-one is prepared following the procedure set forth in part (A) above, but substituting N-benzyl-2-(propanoylamino)-benzamide for N-(1-benzoylethyl)-2-(formylamino)-benzamide (“Compound E”). Compound E is brominated by heating in acetic acid with bromine to provide 2-(1-bromoethyl)-3-benzyl-quinazolin-4-one (“Compound F”). Compound F is treated with 4-methoxy-aniline in triethylamine to provide 2-(1-(4-methoxyphenylamino)ethyl)-3-benzyl-quinazolin-4-one (“Compound G”). Compound G is then acylated with benzoyl chloride to provide 2-(1-(N-benzoyl-N-(4-methoxyphenyl)-aminoethyl)-3-benzyl-quinazolin-4-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07053216B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-2bdfa055382e4b6b99ac6a1a90267c91 |
| Source note | uspto-grants-2006_05 |