HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235634Generated: October 31, 2026
1-(4-Fluorophenyl)piperazine → HCID 13784684, compound
https://huagongshe.com/reaction/235634
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-Fluorophenyl)piperazine | HCID 75260 | — |
| Reactant | HCID 13784632 | HCID 13784632 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 13784684 | HCID 13784684 | — |
Reaction Steps
In 10 ml of ethyl acetate were dissolved 435 mg of 2-(4-chlorobutyl)-2H-1,4-benzothiazin-3(4H)-one and 613 mg of 1-(4-fluorophenyl)piperazine. The solvent was evaporated off, and the residue was stirred at 110° C. for one hour. The reaction mixture was extracted with ethyl acetate, and the extract was washed with water and dried (MgSO4). After removal of the solvent, the residue was subjected to a column chromatography on silica-gel (40 g). From the eluate with hexane-ethyl acetate (1:1, v/v) was obtained 2-[4-[4-(4-fluorophenyl)-1-piperazinyl]butyl]-2H-1,4-benzothiazin-3(4H)-one. The yield was 293 mg (43.2%). Recrystallization from methanol gave prisms, m.p. 150°-151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04640916 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-a14e84e5bd084f6cbf3fecf79c2cbbdc |
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| Source note | uspto-grants-1987_02 |
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