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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959847Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 86608764, compound

https://huagongshe.com/reaction/1959847

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant3-(1-Acetylpiperidin-4-yl)-2-benzothiazol-2-yl-3-hydroxyacrylonitrileHCID 136335806—
SolventDichloromethaneHCID 6344—
ProductHCID 86608764HCID 8660876423%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410272B2
Source datasetuspto-grants-2013_04
ORD IDord-78d8ba3d5ccd414789ce64681bf1434c
Source noteuspto-grants-2013_04