HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235630Generated: October 26, 2026
1-(4-Fluorophenyl)piperazine → 2-[2-[4-(4-fluorophenyl)-1-pyrazinyl]ethyl]-2H-1,4-benzothiazin-3(4H)-one
https://huagongshe.com/reaction/235630
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-Fluorophenyl)piperazine | HCID 75260 | — |
| Reactant | 2-(2-bromoethyl)-3,4-dihydro-2H-1,4-benzothiazin-3-one | HCID 13784623 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-[2-[4-(4-fluorophenyl)-1-pyrazinyl]ethyl]-2H-1,4-benzothiazin-3(4H)-one | HCID 20220108 | — |
Reaction Steps
In 20 ml of ethyl acetate were dissolved 1.36 g of 2-(2-bromoethyl)-2H-1,4-benzothiazin-3(4H)-one and 1.8 g of 1-(4-fluorophenyl)piperazine. The solvent was evaporated off, and the residue was stirred at 110° C. for one hour. The reaction product was extracted with ethyl acetate, and the extract was washed with water and dried over MgSO4. The crystals obtained by evaporation of the solvent were recrystallized from methanol to give 2-[2-[4-(4-fluorophenyl)-1-pyrazinyl]ethyl]-2H-1,4-benzothiazin-3(4H)-one as prisms, m.p. 158°-159° C. The yield was 0.94 g (50.5%).
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-8c226101b90a48d6a2efd64baa8aca18 |
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| Source note | uspto-grants-1987_02 |
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