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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710789Generated: November 3, 2026

Morpholine → 4-{[2-(6-Chloropyridin-3-yl)-4-methyl-1,3-thiazol-5-yl]carbonyl}morpholine

https://huagongshe.com/reaction/1710789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantEthyl 2-(6-chloropyridin-3-yl)-4-methyl-1,3-thiazole-5-carboxylateHCID 59457501—
SolventDichloromethaneHCID 6344—
Product4-{[2-(6-Chloropyridin-3-yl)-4-methyl-1,3-thiazol-5-yl]carbonyl}morpholineHCID 5945749790%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of ethyl 2-(6-chloropyridin-3-yl)-4-methyl-1,3-thiazole-5-carboxylate i98 (0.47 g, 1 eq, 1.84 mmol), morpholine (0.19 g, 1.2 eq, 2.21 mmol) and triethylamine (0.5 ml, 2 eq, 3.68 mmol) in dichloromethane (15 ml) is cooled to 0° C. N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.39 g, 1.1 eq, 2.02 mmol) and 1-hydroxybenzotriazole (0.05 g, 0.2 eq, 0.37 mmol) are then added to the solution and the mixture is stirred 24 h at room temperature. The mixture is then washed with water and a saturated solution of aqueous ammonium chloride. The organic layer is dried over magnesium sulfate, filtered and concentrated under vacuum to give 0.53 g of 4-{[2-(6-chloropyridin-3-yl)-4-methyl-1,3-thiazol-5-yl]carbonyl}morpholine i99.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790720B2
Source datasetuspto-grants-2010_09
ORD IDord-067f455cf5b04987815cd92a1c7f284b
Source noteuspto-grants-2010_09