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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597252Generated: November 3, 2026

Triphenylphosphine → 7-(3-(1,1-Dioxothiomorpholino)propoxy)4-(2-methoxyethylsulphanyl)quinazoline

https://huagongshe.com/reaction/1597252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-(3-Hydroxypropyl)thiomorpholine 1,1-DioxideHCID 11435473—
Reactant7-Hydroxy-4-(2-methoxyethylsulphanyl)quinazolineHCID 135798751—
SolventDichloromethaneHCID 6344—
Product7-(3-(1,1-Dioxothiomorpholino)propoxy)4-(2-methoxyethylsulphanyl)quinazolineHCID 6946276241.7%

Reaction Steps

Diethyl azodicarboxylate (100 μl; 0.63 mmol) was added dropwise to a solution of 7-hydroxy-4-(2-methoxyethylsulphanyl)quinazoline (100 mg, 0.42 mmol), (prepared as described for the starting material in Example 11), 3-(1,1-dioxothiomorpholino)-1-propanol (99 mg, 0.51 mmol) and triphenylphosphine (167 mg, 0.63 mmol) in methylene chloride (6 ml). After stiring for 4 hours, triphenylphosphine (167 mg, 0.63 mmol) and diethyl azodicarboxylate (100 μl, 0.63 mmol) were added and stirring was continued for 1 hour. The volatiles were removed by evaporation and the residue was purified by column chromatography eluting with ethyl acetate/methanol (100/0 followed by 92/8). After removal of the solvent by evaporation, the residue was triturated with ether and the solid was collected by filtration and dried under vacuum to give 7-(3-(1,1-dioxothiomorpholino)propoxy)4-(2-methoxyethylsulphanyl)quinazoline (72 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294532B1
Source datasetuspto-grants-2001_09
ORD IDord-5b08e7463a6d48068e245111785944e6
Source noteuspto-grants-2001_09