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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233266Generated: October 31, 2026

Propargyl alcohol → 4-(Methylthio)-6-methoxy-7-(3-hydroxyprop-1-ynyl)quinazoline

https://huagongshe.com/reaction/2233266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
Reactant4-(Methylthio)-6-methoxy-7-(trifluoromethanesulphonyloxy)quinazolineHCID 86761099—
CatalystTriethylamineHCID 8471—
SolventDimethylformamideHCID 6228—
Product4-(Methylthio)-6-methoxy-7-(3-hydroxyprop-1-ynyl)quinazolineHCID 6867715617%

Reaction Steps

4-(methylthio)-6-methoxy-7-(trifluoromethanesulphonyloxy)quinazoline (1.0 g, 2.82 mmol) in dimethylformamide (30 ml) was reacted with propargyl alcohol (0.51 ml, 8.75 mmol) in the presence of bisdichloro(triphenylphosphine) palladium (100 mg, 0.14 mmol) copper (I) iodide (40 mg) and triethylamine (1.7 ml, 0.0124 mmol) at 90° C. for 2.5 hours under argon. The solvent was evaporated in vacuo, water and hydrochloric acid (2.0 N) were added, and the mixture was extracted with ethyl acetate. Purification by flash chromatography on silica gel, eluting with 7.5% methanol in dichloromethane, yielded 4-(methylthio)-6-methoxy-7-(3-hydroxyprop-1-ynyl)quinazoline (122 mg, 17% yield):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709479B1
Source datasetuspto-grants-2010_05
ORD IDord-42c6ac856b084e63aa63b595414e1d06
Source noteuspto-grants-2010_05