HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365309Generated: October 31, 2026
Potassium Iodide → HCID 23291085, compound
https://huagongshe.com/reaction/365309
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(1-Piperazinylmethyl)quinoline | HCID 4375313 | — |
| Reactant | HCID 23291097 | HCID 23291097 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23291085 | HCID 23291085 | — |
Reaction Steps
A mixture consisting of 7-(3-chloropropoxy)-3,4-dihydro-2H-1,4-benzothiazin-3-one-1-oxide (2.02 g, 7.38 mmol), N-(2-quinolylmethyl)piperazine (2.52 g, 11.07 mmol), potassium carbonate (2.04 g, 14.76 mmol), potassium iodide (2.45 g, 14.76 mmol) and DMF (50 ml) was stirred at 80° C. for 4 hours. The solvent was distilled off from the reaction mixture under reduced pressure, followed by the addition of water. The resulting mixture was extracted with chloroform-methanol (10:1). The extract was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column while using chloroform-ammonia-saturated methanol (10:1) as an eluent. Fractions containing the target compound were collected and then concentrated under reduced pressure, whereby 1.23 g of the title compound was obtained as a yellow oil (4.49 mmol, 60.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127360 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-3376ad834f6d4f3eb24a02d96a54ef7e |
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| Source note | uspto-grants-2000_10 |
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