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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385678Generated: October 30, 2026

Sodium Bicarbonate → HCID 57815432, compound

https://huagongshe.com/reaction/385678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantSodium methanolate methanolHCID 23694274—
ReactantHCID 57815491HCID 57815491—
Reactant1-(2-(4-aminopiperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one hydrochlorideHCID 68927071—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 57815432HCID 5781543239.1%

Reaction Steps

To a suspension of 0.20 g of 1-(2-(4-aminopiperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one hydrochloride in 2 mL of methanol, 0.28 g of a 28% sodium methoxide/methanol solution, 94 mg of 5-fluoro-6-(pyrrolidin-1-yl)nicotinaldehyde and 28 μL of acetic acid were added. Then, 61 mg of sodium cyanoborohydride was added thereto, and the mixture was stirred at room temperature for 2 hours 20 minutes. To the reaction mixture, chloroform, a saturated aqueous sodium hydrogen carbonate solution and water were added. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was washed with water and a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The resultant residue was purified by basic silica gel column chromatography using gradient elution with chloroform:methanol=95:5 to 9:1, thereto was added diethyl ether, and the solid was filtered off to obtain 91 mg of 1-(2-(4-(((5-fluoro-6-(pyrrolidin-1-yl)pyridin-3-yl)methyl)amino)piperidin-1-yl)ethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one as a slightly yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-7464a6def9724eab93359f5003611582
Source noteuspto-grants-2013_02