Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236289Generated: November 1, 2026

6-(Morpholino)pyridin-3-amine → 2-(2-Chloro-phenyl)-4-ethyl-oxazole-5-carboxylic acid (6-morpholin-4-yl-pyridin-3-yl)-amide

https://huagongshe.com/reaction/2236289

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(Morpholino)pyridin-3-amineHCID 104059—
Reactant2-(2-Chloro-phenyl)-4-ethyl-oxazole-5-carboxylic acid 2,5-dioxo-pyrrolidin-1-yl esterHCID 59301312—
SolventAcetonitrileHCID 6342—
Product2-(2-Chloro-phenyl)-4-ethyl-oxazole-5-carboxylic acid (6-morpholin-4-yl-pyridin-3-yl)-amideHCID 5930138352%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 2-(2-chloro-phenyl)-4-ethyl-oxazole-5-carboxylic acid 2,5-dioxo-pyrrolidin-1-yl ester (174 mg, 0.5 mmol) and 6-morpholin-4-yl-pyridin-3-ylamine (90 mg, 0.5 mmol) in 5 mL of acetonitrile was stirred at 85° C. overnight. The solvent was removed in vacuo, and the crude product was purified by flash chromatography (Merck silica gel 60, 230-400 mesh, 0-15% methanol in methylene chloride for 30 min) to yield 2-(2-chloro-phenyl)-4-ethyl-oxazole-5-carboxylic acid (6-morpholin-4-yl-pyridin-3-yl)-amide (107 mg, 52% yield) as a light yellow solid. LCMS calcd for C21H21ClN4O3 (m/e) 412, obsd 413 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714126B2
Source datasetuspto-grants-2010_05
ORD IDord-3692a06edec3478cb853a9e9c6441f13
Source noteuspto-grants-2010_05