HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855694Generated: October 26, 2026
Triphenylphosphine → 7-(2-(Imidazol-1-yl)ethoxy)-6-methoxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one
https://huagongshe.com/reaction/855694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-(2-Hydroxyethyl)imidazole | HCID 74168 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (7-Hydroxy-6-methoxy-4-oxoquinazolin-3(4H)-yl)methyl pivalate | HCID 10804576 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-(2-(Imidazol-1-yl)ethoxy)-6-methoxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one | HCID 22030782 | 80% |
Reaction Steps
Diethyl azodicarboxylate (435 mg, 2.5 mmol) was added dropwise to a suspension of 7-hydroxy-6-methoxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one (612 mg, 2 mmol), 2-(imidazol-1-yl)ethanol (280 mg, 2.5 mmol), (J. Med. Chem. 1993, 25, 4052-4060), and triphenylphosphine (655 mg, 2.5 mmol) in methylene chloride (10 ml) at 5° C. The mixture was stirred for 10 minutes at 5° C. and then 1 hour at ambient temperature. The mixture was poured directly on to a silica column and eluted with methylene chloride/methanol (95/5) to give 7-(2-(imidazol-1-yl)ethoxy)-6-methoxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one (640 mg, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07262201B1 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-f932b3dd36fb4a3096e30ede7f7057fc |
|---|
| Source note | uspto-grants-2007_08 |
|---|