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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550802Generated: October 29, 2026

Sodium Bicarbonate → HCID 67197212, compound

https://huagongshe.com/reaction/550802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantAcetaldehyde ammoniaHCID 522583—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 67197393HCID 67197393—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 67197212HCID 67197212—

Reaction Steps

A mixture of 400 mg of 1-[2-(4-chloro-2,5-difluorophenyl)-6,6-dioxido-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl]piperidin-4-one, 10 ml of methylene chloride, 65 μl of aminoethanol, and two drops of acetic acid was stirred at ambient temperature for 1 hour, here was then added 617 mg of sodium triacetoxyborohydride, and the mixture was stirred at ambient temperature for 3 hours. Saturated aqueous sodium bicarbonate was added to the reaction mixture, and the resultant mixture was extracted with chloroform-THF mixed solvent. The organic phase obtained was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue obtained was dissolved in THF-MeOH, here was added 4M HCl-dioxane solution, the solution was concentrated under reduced pressure, and the residue was recrystallized from EtOH-acetonitrile to yield 426 mg of 2-({1-[2-(4-chloro-2,5-difluorophenyl)-6,6-dioxido-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl]piperidin-4-yl}amino)ethanol dihydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947690B2
Source datasetuspto-grants-2011_05
ORD IDord-332f0010d3084ac49e14a895a2d7abe6
Source noteuspto-grants-2011_05