HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389286Generated: October 28, 2026
1-Methylpiperazine → 3-Fluoro-8-isopropyl-10-(4-methylpiperazino)-10,11-dihydrodibenzo(b,f)thiepin
https://huagongshe.com/reaction/1389286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | 3-fluoro-8-isopropyldibenzo(b,f)thiepin-10(11H)-one | HCID 826394 | — |
| Reactant | 3-Fluoro-8-isopropyl-10-(4-methylpiperazino)dibenzo(b,f)thiepin | HCID 3054175 | — |
| Reactant | Maleate(2-) | HCID 5288227 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Fluoro-8-isopropyl-10-(4-methylpiperazino)-10,11-dihydrodibenzo(b,f)thiepin | HCID 3054166 | — |
Reaction Steps
A stirred solution of 8.0 g 3-fluoro-8-isopropyldibenzo(b,f)thiepin-10(11H)-one in 55 ml benzene is treated with a solution of 2.8 g titanium tetrachloride in 14 ml benzene added dropwise. 14 g of 1-methylpiperazine are then slowly added and the mixture refluxed for 16 hours. After cooling, it is decomposed with 80 ml water, added dropwise. 100 ml benzene are then added and the separated solid is filtered. The benzene layer of the filtrate is washed with water, dried with potassium carbonate and evaporated. There are obtained 9.2 g (89%) crude oily base which is neutralized with maleic acid in ethanol. Addition of ether separates the crystalline maleate of 3-fluoro-8-isopropyl-10-(4-methylpiperazino)dibenzo(b,f)thiepin melting at 183°-184° C. with decomposition (ethanol-ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04243805 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-9185e63d697445ea99dfb04f0363baca |
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| Source note | uspto-grants-1981_01 |
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