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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330800Generated: October 30, 2026

Water → 3-{3-[5-(2-morpholin-4-ylethoxy)pyrimidin-2-yl]benzyl}-5-trifluoromethyl-3H-benzothiazol-2-one

https://huagongshe.com/reaction/330800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(Trifluoromethyl)benzo[d]thiazol-2(3H)-oneHCID 13227340—
Reactant4-{2-[2-(3-Chloromethylphenyl)pyrimidin-5-yloxy]ethyl}morpholine hydrochlorideHCID 66985501—
SolventAcetonitrileHCID 6342—
Product3-{3-[5-(2-morpholin-4-ylethoxy)pyrimidin-2-yl]benzyl}-5-trifluoromethyl-3H-benzothiazol-2-oneHCID 46700771—

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of 89 mg (0.405 mmol) of 5-trifluoromethyl-3H-benzothiazol-2-one, 150 mg (0.405 mmol) of 4-{2-[2-(3-chloromethylphenyl)pyrimidin-5-yl-oxy]ethyl}morpholine hydrochloride and 286 mg (2.02 mmol) of potassium carbonate in 8 ml of acetonitrile are stirred at 70° C. for 5 days. 30 ml of water are added to the reaction mixture, with a precipitate slowly forming. The precipitate is filtered off with suction, washed with water and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877751B2
Source datasetuspto-grants-2014_11
ORD IDord-d6e890e927a2402ab0aae87c0d87fe88
Source noteuspto-grants-2014_11