HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729314Generated: October 30, 2026
1,3-Dimethyl-6-(piperazin-1-yl)pyrimidine-2,4(1H,3H)-dione → HCID 19011765, compound
https://huagongshe.com/reaction/1729314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dimethyl-6-(piperazin-1-yl)pyrimidine-2,4(1H,3H)-dione | HCID 12816873 | — |
| Reactant | HCID 22988732 | HCID 22988732 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19011765 | HCID 19011765 | 163.3% |
Reaction Steps
A mixture of 1 g of 2-(2-methanesulfonyloxyphenyl)ethylmethane sulfonate and 0.65 g of 1,3-dimethyl-6-(piperazin-1-yl)-2,4(1H,3H)-pyrimidinedione was stirred at 90° C. for 2 hours and then allowed to stand for cooling. The resultant reaction mixture was dissolved in 50 ml of chloroform, and then washed with 10 ml of a 1N aqueous sodium hydroxide solution. The chloroform layer was washed with water, dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the residue was purified through a silica gel column chromatograph (chloroform/methanol=40/1 in volume ratio), thereby obtaining 2.0 g of 1,3-dimethyl-6-[4-(2-[2-methanesulfonyloxyphenyl]ethyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05332739 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-ba58be98ec844d3cb21ebd9aca9c1a98 |
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| Source note | uspto-grants-1994_07 |
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