HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235629Generated: October 31, 2026
1-(2-Methoxyphenyl)piperazine → HCID 13784664, compound
https://huagongshe.com/reaction/235629
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | HCID 13784628 | HCID 13784628 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13784664 | HCID 13784664 | 26.6% |
Reaction Steps
In 10 ml of dimethylformamide were dissolved 1.6 g of 2-(3-chloropropyl)-2H-1,4-benzothiazin-3(4H)-one and 2.55 g of 1-(2-methoxyphenyl)piperazine. The solution was stirred at 100° C. for 1.5 hour. The reaction mixture was poured into ice-water, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over MgSO4, then concentrated under reduced pressure. The concentrate was subjected to a column chromatography on silica-gel (150 g). From the eluate with hexane-acetone (2:1, v/v) was obtained 0.7 g of 2-[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]-2H-1,4-benzothiazin-3(4H)-one as an oily substance. The 3/2 oxalate of this product was obtained as crystals, which were recrystallized from methanol and dichloromethane to give colorless prisms. The yield was 470 mg (13.3%), m.p. 202°-204° 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-9c496464800148e1a22c2a96767171be |
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| Source note | uspto-grants-1987_02 |
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