HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855697Generated: October 27, 2026
Diethylene Glycol Monomethyl Ether → HCID 22030859, compound
https://huagongshe.com/reaction/855697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylene Glycol Monomethyl Ether | HCID 8134 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| 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 | HCID 22030859 | HCID 22030859 | 106.7% |
Reaction Steps
Diethyl azodicarboxylate (864 μl, 5.5 mmol) was added dropwise to a mixture of 7-hydroxy-6-methoxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one 1.2 g, 3.9 mmol) (prepared as described for the starting material in Example 7), triphenylphosphine (1.44 g, 5.5 mmol) and 2-(2-methoxyethoxy)ethanol (653 μl, 5.5 mmol) in methylene chloride (70 ml) cooled at 0° C. The mixture was stirred for 1.5 hours at ambient temperature and the solvent was removed by evaporation. The residue was purified by column chromatography eluting with a mixture of ethyl acetate/methylene chloride (50/50 followed by 80/20). The purified solid was suspended in ether, collected by filtration and dried under vacuum to give 6-methoxy-7-(2-(2-methoxyethoxy)ethoxy)-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one (1.70 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262201B1 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-087596c8185b4c98a10f522d920707d7 |
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| Source note | uspto-grants-2007_08 |
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