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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442002Generated: October 29, 2026

3-[2-(1-Piperazinyl)ethyl]-2-oxazolidinone → HCID 21416103, compound

https://huagongshe.com/reaction/442002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[2-(1-Piperazinyl)ethyl]-2-oxazolidinoneHCID 12275545—
ReactantHCID 21416161HCID 21416161—
SolventChloroformHCID 6212—
ProductHCID 21416103HCID 21416103—

Reaction Steps

20 G. of 2,10-dichloro-10,11-dihydro-7-methyl-dibenzo[b,f]thiepin are stirred with 41 g. of 3-[2-(1-piperazinyl)-ethyl]-2-oxazolidinone and 400 ml. of chloroform at the boiling temperature for 20 hours. The solution is cooled and washed successively with 2N sodium hydroxide and with water. The organic phase is decanted and extracted with dilute methanesulfonic acid. The acid solution is made alkaline with sodium hydroxide and the oil which separates out is shaken out with ether. The ether solution is washed with water, dried over magnesium sulfate and evaporated under reduced pressure, whereby there is obtained 3-{2-[4-(2-chloro-10,11-dihydro-7-methyl-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl}-2-oxazolidinone (melting point 161°-163° C.) which is converted into the corresponding dimethanesulfonate (melting point 187°-189° C.) by reaction with methanesulfonic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04044010
Source datasetuspto-grants-1977_08
ORD IDord-64558a6929a64810b9811b0d6b179d66
Source noteuspto-grants-1977_08