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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78538Generated: November 2, 2026

Dichloromethane → 5-methyl-3-(2-morpholinoethyl)thiazol-2(3H)-imine

https://huagongshe.com/reaction/78538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
Reactant2-Amino-5-methylthiazoleHCID 351770—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductAmmonium HydroxideHCID 14923—
Product5-methyl-3-(2-morpholinoethyl)thiazol-2(3H)-imineHCID 6862341488.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-amino-5-methylthiazole (1.0 g, 8.8 mmol), 4-(2-chloroethyl)-morpholine hydrochloride (1.7 g, 9.2 mmol) and Et3N (3.7 mL, 26 mmol) in DMF (5 mL) was warmed to 80° C. and was allowed to stir for 24 h. The mixture was then cooled to ambient temperature, quenched with saturated aqueous NaHCO3 (5 mL), and diluted with CH2Cl2 (5 mL). The layers were separated and the aqueous layer was extracted with CH2Cl2 (3×5 mL). The combined organics were dried over anhydrous Na2SO4, filtered, concentrated under reduced pressure and purified via column chromatography (SiO2, 10% CH3OH in EtOAc then 9:1:0.1 CH2Cl2:CH3OH:NH4OH) to give the title compound (0.88 g, 3.9 mmol, 44% yield). MS (DCI/NH3) m/z 228 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841334B2
Source datasetuspto-grants-2014_09
ORD IDord-1e19bda0b23f4a049223573c0023ef3a
Source noteuspto-grants-2014_09