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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-[2-(1-Piperazinyl)ethyl]-2-oxazolidinone | HCID 12275545 | — |
| Reactant | HCID 21416161 | HCID 21416161 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21416103 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04044010 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-64558a6929a64810b9811b0d6b179d66 |
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| Source note | uspto-grants-1977_08 |
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