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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349949Generated: October 29, 2026

Triethylamine → 5-(2-(Methanesulfonyloxy)ethoxy)-2-methylquinazoline

https://huagongshe.com/reaction/1349949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 17965146HCID 17965146—
SolventDichloromethaneHCID 6344—
Product5-(2-(Methanesulfonyloxy)ethoxy)-2-methylquinazolineHCID 1796513999%

Reaction Steps

To a solution of 2-(2-methylquinazolin-5-yloxy)ethanol (0.330 g, 1.62 mmol) in dichloromethane (20 mL) and triethylamine (0.34 mL, 2.43 mmol) was added methane sulfonyl chloride (0.14 mL, 1.78 mmol) dropwise. The reaction mixture was allowed to stir at room temperature for 2 h. The reaction mixture was diluted with further dichloromethane and partitioned with saturated NaHCO3 aq. The organic phase was washed with brine, dried (MgSO4) and evaporated in vacuo to give the title compound as a cream solid (0.452 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214674B2
Source datasetuspto-grants-2007_05
ORD IDord-67a60fbbd19a4a8faa04c4f341ee8969
Source noteuspto-grants-2007_05