HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442000Generated: October 29, 2026
Sodium Hydroxide → HCID 21416148, compound
https://huagongshe.com/reaction/442000
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-[2-(1-Piperazinyl)ethyl]-2-oxazolidinone | HCID 12275545 | — |
| Reactant | HCID 21416164 | HCID 21416164 | — |
| Product | HCID 21416148 | HCID 21416148 | — |
Reaction Steps
17 G. of 3,10-dichloro-7-fluoro-10,11-dihydro-dibenzo[b,f]thiepin are treated with 45.5 g. of 3-[2-(1-piperazinyl)-ethyl]-2-oxazolidinone and stirred at 120°-130° C. (internal temperature) for 8 minutes. The mixture is treated with 2N sodium hydroxide and extracted with ether. The ether solution is washed to neutrality and shaken out with dilute methanesulfonic acid. The acid solution is made alkaline with sodium hydroxide and extracted with methylene chloride. The organic solution is washed with water and dried over magnesium sulfate. The residue is recrystallized from acetone, whereby there is obtained 3-{2-[4-(3-chloro-7-fluoro-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl}-2-oxazolidinone (melting point 168°-170° C.) which is converted into the dimethanesulfonate (melting point 191°-193° C.) by reaction with methansulfonic 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-f812c6632fd841cabbcd468798556f6f |
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| Source note | uspto-grants-1977_08 |
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