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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943610Generated: November 2, 2026

Pyridine → HCID 74017985, compound

https://huagongshe.com/reaction/1943610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 58978939HCID 58978939—
ProductHCID 74017985HCID 7401798560%

Reaction Conditions

Temperature0 °C

Reaction Steps

P-toluenesulfonyl chloride (210 mg, 1.10 mmol) is added to a solution of (E)-2-(6,7-dihydro-1-phenyl-1H-indazol-4(5H)-ylidene)ethanol (254 mg, 1.05 mmol) in 10 mL de pyridine cooled to a 0° C. The reaction is followed up by TLC. Next, the solvent is evaporated, the crude is diluted with CHCl3, and washed with a diluted solution of NaHCO3. The organic phase is evaporated at reduced pressure, to obtain 1-[2-(1-phenyl-1,5,6,7-tetrahydroindazol-4-ylidene)-ethyl]-pyridinium toluene-4-sulfonate (300 mg, 0.63 mmol, 60%, yellow solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394797B2
Source datasetuspto-grants-2013_03
ORD IDord-643128285de64cb7a05eaff54cc630e2
Source noteuspto-grants-2013_03