HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279664Erstellt: 24. Oktober 2026
Triphenylphosphine → 7-(2-(Imidazol-1-yl)ethoxy)-6-methoxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one
https://huagongshe.com/de/reaction/279664
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | N-(2-Hydroxyethyl)imidazole | HCID 74168 | — |
| Edukt | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Edukt | (7-Hydroxy-6-methoxy-4-oxoquinazolin-3(4H)-yl)methyl pivalate | HCID 10804576 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 7-(2-(Imidazol-1-yl)ethoxy)-6-methoxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one | HCID 22030782 | 80% |
Reaktionsschritte
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), (prepared as described for the starting material in Example 85), 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%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06362336B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-d9c62763225047ae9a0430a506c014f0 |
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| Quellennotiz | uspto-grants-2002_03 |
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