HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437831Generated: October 30, 2026
HCID 22767879, compound → HCID 22767919, compound
https://huagongshe.com/reaction/437831
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22767879 | HCID 22767879 | — |
| Reactant | HCID 22767948 | HCID 22767948 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22767919 | HCID 22767919 | — |
Reaction Steps
A solution of 3 g. of 10-chloro-10,11-dihydro-2-methyl-8-methylthio-dibenz[ b,f]oxepin and 5.73 g. of 1-[2-(1-piperazinyl)-ethyl]-2-piperidone in 18 ml. of chloroform is heated at reflux for 20 hours. The solvent is removed in vacuo. The residue is partitioned between benzene and 10% aqueous sodium carbonate solution. The benzene solution is extracted with dilute hydrochloric acid. The acid-aqueous solution is made alkaline with sodium bicarbonate and extracted with benzene. The benzene extract is washed several times with water, dried, evaporated in vacuo, and there is obtained 1-[2-{4-[10,11-dihydro-2-methyl-8-methylthio-dibenz[b,f]oxepin-10-yl]-1-piperazinyl}-ethyl]-2-piperidone. The dihydrochloride is prepared in ethanol by the addition of an excess of alcoholic hydrogen chloride. By the addition of ether, there are obtained crystals having a melting point of 183°-185° C. (with decomposition). By re-dissolving the dihydrochloride in water, there is obtained the monohydrochloride having a melting point of 117°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04032525 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-b743e18a89df40e290f310486ba6ce3f |
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| Source note | uspto-grants-1977_06 |
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