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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597249Generated: October 31, 2026

Triphenylphosphine → 4-Methylsulphanyl-7-(4-morpholinobut-2-en-1-yloxy)quinazoline

https://huagongshe.com/reaction/1597249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-Morpholinobut-2-en-1-olHCID 53926128—
Reactant7-Hydroxy4-methylsulphanylquinazolineHCID 135674019—
SolventDichloromethaneHCID 6344—
Product4-Methylsulphanyl-7-(4-morpholinobut-2-en-1-yloxy)quinazolineHCID 5369723355.5%

Reaction Steps

Using a procedure analogous to the one described for the synthesis of the starting material in Example 16, 4-morpholinobut-2-en-1-ol (1.27 g, 8.13 mmol), (J. Med. Chem. 1972, 15, 110-112), was reacted with 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) in the presence of triphenylphosphine (4.09 g, 1.56 mmol) and diethyl azodicarboxylate (2.46 ml, 1.56 mmol) to give 4-methylsulphanyl-7-(4-morpholinobut-2-en-1-yloxy)quinazoline (1.15 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294532B1
Source datasetuspto-grants-2001_09
ORD IDord-7ea7870dcb114cb8a9db38d038fdd17f
Source noteuspto-grants-2001_09