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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-Morpholinobut-2-YN-1-OLHCID 3112849—
Reactant7-Hydroxy4-methylsulphanylquinazolineHCID 135674019—
SolventDichloromethaneHCID 6344—
Product4-Methylsulphanyl-7-(4-morpholinobut-2-yn-1-yloxy)quinazolineHCID 2264929663.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294532B1
Source datasetuspto-grants-2001_09
ORD IDord-15c47e07f5e145b5834ab978007c6088
Source noteuspto-grants-2001_09