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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Aminomorpholine | HCID 20315 | — |
| Reactant | 1-(2-Chloropyridine-3-carbonyl)-2-methylthio-2-imidazoline | HCID 14387135 | — |
| Product | 2,10-dihydro-10-(4-morpholinyl)imidazo[1,2-a]pyrido[2,3-d]pyrimidin-5(3H)-one | HCID 14387136 | 52% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04871732 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-d043a53d9458470d8252831e938c34db |
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| Source note | uspto-grants-1989_10 |
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