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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707524Generated: October 31, 2026

Sodium Thiosulfate → 6-(3-(4-Ethylpiperazin-1-yl)azetidin-1-yl)-5-fluoropyridine-2-carbaldehyde

https://huagongshe.com/reaction/707524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
Reactant(6-(3-(4-Ethylpiperazin-1-yl)azetidin-1-yl)-5-fluoropyridin-2-yl)methanolHCID 118162492—
SolventDichloromethaneHCID 6344—
Product6-(3-(4-Ethylpiperazin-1-yl)azetidin-1-yl)-5-fluoropyridine-2-carbaldehydeHCID 118162455—

Reaction Steps

To a mixed solution of the crude product (402 mg) of (6-(3-(4-ethylpiperazin-1-yl)azetidin-1-yl)-5-fluoropyridin-2-yl)methanol described in Production Example 7-1 and dichloromethane (10.0 mL) was added Dess-Martin periodinane (787 mg, 1.86 mmol) at room temperature. The resultant mixture was stirred at room temperature for 2 hours. A saturated aqueous sodium thiosulfate solution and a saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture, and the resultant solution was extracted with dichloromethane. An organic layer was dried over anhydrous magnesium sulfate and then filtrated. The solvent was evaporated under a reduced pressure to give a crude product (362 mg) of the title compound. The product was used in the subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174998B2
Source datasetuspto-grants-2015_11
ORD IDord-3e84755133444c8890539bfaa4c6f992
Source noteuspto-grants-2015_11