HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651042Generated: October 25, 2026
1-(2-Methoxyphenyl)piperazine → HCID 15136107, compound
https://huagongshe.com/reaction/1651042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | 3-ethoxycarbonyl-9-mercapto-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 14306471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15136107 | HCID 15136107 | — |
Reaction Steps
To a solution of 1.0 g (4 mmol) of 3-ethoxycarbonyl-9-mercapto-4-oxo-4H-pyrido[1,2-a]pyrimidine (II-1) in 40 ml of dry methylene chloride is added 0.24 ml (2 mmol) of trichloromethyl chloroformate, and the resultant mixture is stirred for 10 min. and concentrated at room temperature under atmospheric pressure. To the residue are added 60 ml of dry methylene chloride and 0.77 ml (44 mmol) of 4-(2-methoxyphenyl)piperazine under ice-cooling, and the reaction mixture is stirred for 1 hour at room temperature. The reaction mixture is washed with N--HCl, saturated aqueous NaHCO3 and water in order, and the organic layer is dried and concentrated under reduced pressure. The oily residue in 1.94 g is chromatographed on a column of silica gel eluting with ethyl acetate to give 45 mg of Ia-2 (m.p. 154°-156° C. recrystallized from chloroform-n-hexane) and 516 mg of IV-2 (m.p. 151°-153° C. recrystallized from ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04927829 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-a0e0a7cd77664a41a400a8721b477e46 |
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| Source note | uspto-grants-1990_05 |
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