HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280569Generated: November 1, 2026
Ethyl 4-amino-1-piperidinecarboxylate → 3-(2-chlorophenyl)-7-(1-ethoxycarbonylpiperidin-4-ylamino)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one
https://huagongshe.com/reaction/1280569
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-amino-1-piperidinecarboxylate | HCID 100867 | — |
| Reactant | 3-(2-chlorophenyl)-7-benzylsulfonyl-3,4-dihydropyrimido[4,5-d]-pyrimidin-2(1H)-one | HCID 18002474 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(2-chlorophenyl)-7-(1-ethoxycarbonylpiperidin-4-ylamino)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one | HCID 18425466 | 54.8% |
Reaction Steps
Sulfone 9.1 (1.0 g, 2.41 mmol) was taken up in 5 mL ethyl 4-amino-1-piperidinecarboxylate (29 mmol) and stirred at 150° C. After 1 hour, the reaction slurry was cooled to room temperature, poured into 50 mL methanol, and filtered to collect a white solid. The solid was washed with an additional 50 mL methanol and dried in vacuo to yield 0.569 g of 3-(2-chlorophenyl)-7-(1-ethoxycarbonylpiperidin-4-ylamino)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06451804B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-4c108898cb5b4869a3165063a290fdcf |
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| Source note | uspto-grants-2002_09 |
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