HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235628Generated: October 31, 2026
1-(4-Fluorophenyl)piperazine → 2-[3-[4-(4-fluorophenyl)-1-piperazinyl]propyl]-6,7-dimethyl-2H-1,4-benzothiazin-3(4H)-one
https://huagongshe.com/reaction/235628
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-Fluorophenyl)piperazine | HCID 75260 | — |
| Reactant | 2-(3-bromopropyl)-6,7-dimethyl-2H-1,4-benzothiazin-3(4H)-one | HCID 13784613 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-[3-[4-(4-fluorophenyl)-1-piperazinyl]propyl]-6,7-dimethyl-2H-1,4-benzothiazin-3(4H)-one | HCID 13784640 | 78.6% |
Reaction Steps
In 10 ml of ethyl acetate were dissolved 628 mg of 2-(3-bromopropyl)-6,7-dimethyl-2H-1,4-benzothiazin-3(4H)-one and 721 mg of 1-(4-fluorophenyl)piperazine. The solution was concentrated and the concentrate was stirred at 110° C. for one hour, diluted with water, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over MgSO4 and concentrated to give 2-[3-[4-(4-fluorophenyl)-1-piperazinyl]propyl]-6,7-dimethyl-2H-1,4-benzothiazin-3(4H)-one (650 mg, 78.6%). Recrystallization from methanol gave colorless prisms, m.p. 161°-162° 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-00d3682dc3a84113a1e9543fe0a112b5 |
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| Source note | uspto-grants-1987_02 |
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