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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441996Generated: October 30, 2026

3-[2-(1-Piperazinyl)ethyl]-2-oxazolidinone → 3-{2-[4-(8-Fluoro-10,11-dihydro-3-methyl-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl}-2-oxazolidinone

https://huagongshe.com/reaction/441996

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[2-(1-Piperazinyl)ethyl]-2-oxazolidinoneHCID 12275545—
Reactant10-Chloro-8-fluoro-10,11-dihydro-3-methyldibenzo[b,f]thiepinHCID 21416157—
SolventChloroformHCID 6212—
Product3-{2-[4-(8-Fluoro-10,11-dihydro-3-methyl-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl}-2-oxazolidinoneHCID 21416205—

Reaction Steps

10.6 g. of 10-chloro-8-fluoro-10,11-dihydro-3-methyl-dibenzo[b,f]thiepin are heated at reflux together with 200 ml. of chloroform and 22.8 g. of 3-[2-(1-piperazinyl)-ethyl]-2-oxazolidinone for 30 hours. Thereafter, the mixture is evaporated under reduced pressure, and the residue is worked up as described in Example 5. The insoluble base is recrystallized from ethanol, whereby there is obtained 3-{2-[4-(8-fluoro-10,11-dihydro-3-methyl-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl}-2-oxazolidinone which melts at 173°-175° C. The maleate crystallizes from acetone/ether and has a melting point of 147°-149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04044010
Source datasetuspto-grants-1977_08
ORD IDord-4e6cf82ac527423f930f1a9735f88cc5
Source noteuspto-grants-1977_08