HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386320Generated: October 30, 2026
Triphenylphosphine → 7-(3-Morpholinopropoxy)-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one
https://huagongshe.com/reaction/1386320
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Morpholino-1-propanol | HCID 199576 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 7-Hydroxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one | HCID 21699294 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-(3-Morpholinopropoxy)-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one | HCID 21699269 | 68.4% |
Reaction Steps
7-Hydroxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one (750 mg, 2.7 mmol) was suspended in methylene chloride (40 ml) at 5° C. and 4-(3-hydroxypropyl)morpholine (490 mg, 3.4 mmol) and triphenylphosphine (890 mg, 3.4 mmol) were added. The mixture was stirred for 5 minutes and diethyl azodicarboxylate (590 mg, 3.4 mmol) was added over 5 minutes at 5° C. The reaction mixture was stirred at 5° C. for 30 minutes then at ambient temperature for 1 hour. The solution was then purified directly by column flash chromatography eluting with methylene chloride, and then ethyl acetate, acetonitrile/ethyl acetate (20/80), and acetonitrile/ethyl acetate/ammonia (50/50/0.5). The purified product was triturated with ether/isohexane and collected by filtration to give 7-(3-morpholinopropoxy)-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one (745 mg, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265411B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-0ce57726cc7c4e3589fa07c15fa017e6 |
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| Source note | uspto-grants-2001_07 |
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