HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407346Generated: October 29, 2026
4-Toluenesulfonyl chloride → HCID 86608764, compound
https://huagongshe.com/reaction/407346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(1-Acetylpiperidin-4-yl)-2-benzothiazol-2-yl-3-hydroxyacrylonitrile | HCID 136335806 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86608764 | HCID 86608764 | 23% |
Reaction Steps
To a solution of the above prepared 3-(1-acetylpiperidin-4-yl)-2-benzothiazol-2-yl-3-hydroxyacrylonitrile (415 mg, 1.27 mmol) in anhydrous dichloromethane (20 mL) at room temperature under argon were added triethylamine (193 mg, 1.9 mmol) and tosyl chloride (303 mg, 1.59 mmol) in small portions. The resulting mixture was stirred at room temperature for 6 hrs. The reaction mixture was diluted with dichloromethane. The organic phase was washed with 1% HCl, 0.5% NaOH, water, brine, and dried over anhydrous sodium sulfate, filtered, and evaporated. The resulting crude product was purified by flash column chromatography eluting with CH2Cl2:MeOH=20:1 to yield 140 mg (23%) of toluene-4-sulfonic acid 1-(1-acetylpiperidin-4-yl)-2-benzothiazol-2-yl-2-cyanovinyl ester. MS (m/z, ES+): 482.1 (M+1, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754233B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-7c849ce77b0248208d680299c13d385a |
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| Source note | uspto-grants-2014_06 |
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