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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350858Generated: October 26, 2026

N-Aminomorpholine → 2,10-dihydro-10-(4-morpholinyl)imidazo[1,2-a]pyrido[2,3-d]pyrimidin-5(3H)-one

https://huagongshe.com/reaction/2350858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-AminomorpholineHCID 20315—
Reactant1-(2-Chloropyridine-3-carbonyl)-2-methylthio-2-imidazolineHCID 14387135—
Product2,10-dihydro-10-(4-morpholinyl)imidazo[1,2-a]pyrido[2,3-d]pyrimidin-5(3H)-oneHCID 1438713652%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 5.00 g (19.5 mmoles) of the product of Example 12 and 6.40 g (62.6 mmoles) of N-aminomorpholine was heated in an oil bath at 160° C. for 1 hour. The resulting mixture was cooled and partitioned between methylene chloride and water. The organic layer was dried (sodium sulfate) and concentrated. The crystalline residue was triturated with hexane. The resulting solid was collected to give 2.75 g of 2,10-dihydro-10-(4-morpholinyl)imidazo[1,2-a]pyrido[2,3-d]pyrimidin-5(3H)-one. Melting point 225°-226° C. Total yield 52%. This compound exhibits the following formula: ##STR9##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871732
Source datasetuspto-grants-1989_10
ORD IDord-d043a53d9458470d8252831e938c34db
Source noteuspto-grants-1989_10