HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785430Generated: October 27, 2026
4-Methylmorpholine → HCID 57593178, compound
https://huagongshe.com/reaction/1785430
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 3-(2-Aminopropyl)benzyl alcohol | HCID 24721512 | — |
| Reactant | HCID 57593124 | HCID 57593124 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57593178 | HCID 57593178 | — |
Reaction Steps
A mixture of 9-(2-methanesulfonyl-pyrimidin -4-yl)-2-phenyl-6,7,8,9-tetrahydro-pyrimido[1,2-a]pyrimidin-4-one (344 mg, 0.90 mmol), [3-(2-amino-propyl)-phenyl]-methanol (371 mg, 2.25 mmol), and N-methylmorpholine (8 mL) was heated to 100° C. for 20 h. Reaction was diluted with dichloromethane (15 mL) and ethyl acetate (40 mL), washed three times with water (50 mL) then saturated sodium chloride (10 mL). Organic dried over magnesium sulfate then concentrated to a oil under vacuum. Product purified on silica and isolated as a white solid. M+1=469.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504403B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-9d93330cbfb24dd48d5ecbd2a97476b6 |
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| Source note | uspto-grants-2009_03 |
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