HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597248Generated: November 2, 2026
Triphenylphosphine → 4-Methylsulphanyl-7-(4-morpholinobut-2-yn-1-yloxy)quinazoline
https://huagongshe.com/reaction/1597248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 4-Morpholinobut-2-YN-1-OL | HCID 3112849 | — |
| Reactant | 7-Hydroxy4-methylsulphanylquinazoline | HCID 135674019 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methylsulphanyl-7-(4-morpholinobut-2-yn-1-yloxy)quinazoline | HCID 22649296 | 63.1% |
Reaction Steps
Triphenylphosphine (4.09 g, 1.56 mmol) was added dropwise to a solution of 7-hydroxy-4-methylsulphanylquinazoline (1.2 g, 6.25 mmol), (prepared as described for the starting material in Example 8), in methylene chloride (30 ml), followed by 4-morpholinobut-2-yn-1-ol (1.26 g, 8.3 mmol), (J. Am. Chem. Soc. 1957, 79, 6184), in methylene chloride (5 ml) and diethyl azodicarboxylate (2.46 ml, 1.56 mmol) was added dropwise. After stirring for 3 hours at ambient temperature, the volatiles were removed under vacuum and the residue was purified by column chromatography eluting with methylene chloride/methanol (100/0 followed by 95/5). After removal of the solvent, the residue was triturated with ether, collected by filtration and dried under vacuum to give 4-methylsulphanyl-7-(4-morpholinobut-2-yn-1-yloxy)quinazoline (1.3 g, 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06294532B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-15c47e07f5e145b5834ab978007c6088 |
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| Source note | uspto-grants-2001_09 |
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