Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantDiphosgeneHCID 10426—
Reactant3-ethoxycarbonyl-9-mercapto-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 14306471—
SolventDichloromethaneHCID 6344—
ProductHCID 15136107HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927829
Source datasetuspto-grants-1990_05
ORD IDord-a0e0a7cd77664a41a400a8721b477e46
Source noteuspto-grants-1990_05