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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491072Generated: October 25, 2026

Water → 4-chloro-2-(N-(2-morpholin-4-ylethyl)carbamoyl)pyridine

https://huagongshe.com/reaction/491072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-MorpholinoethylamineHCID 408285—
ReactantMethyl 4-chloropyridine-2-carboxylate--hydrogen chloride (1/1)HCID 16655470—
SolventTetrahydrofuranHCID 8028—
Product4-chloro-2-(N-(2-morpholin-4-ylethyl)carbamoyl)pyridineHCID 2361457995.4%

Reaction Steps

To a solution of methyl 4-chloropyridine-2-carboxylate HCl salt (Method A2, Step 2; 1.01 g, 4.86 mmol) in THF (20 mL) was added 4-(2-aminoethyl)morpholine (2.55 mL, 19.4 mmol) dropwise and the resulting solution was heated at the reflux temp. for 20 h, cooled to room temp., and treated with water (50 mL). The resulting mixture was extracted with EtOAc (50 mL). The organic layer was dried (MgSO4) and concentrated under reduced pressure to afford 4-chloro-2-(N-(2-morpholin-4-ylethyl)carbamoyl)pyridine as a yellow oil (1.25 g, 95%): TLC (10% MeOH/90% EtOAc) Rf0.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528255B2
Source datasetuspto-grants-2009_05
ORD IDord-6242253afe50426fb3d68246df44c185
Source noteuspto-grants-2009_05