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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39793Generated: October 29, 2026

Sodium Bicarbonate → HCID 59398427, compound

https://huagongshe.com/reaction/39793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(piperidin-4-yl)-2,3-dihydro-1,4-benzodioxin-6-carboxamideHCID 28938004—
Reactant(2-oxoquinoxalin-1(2H)-yl)acetaldehydeHCID 59397888—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 59398427HCID 5939842774.2%

Reaction Steps

To 3 mL of dichloromethane solution containing 70 mg of (2-oxoquinoxalin-1(2H)-yl)acetaldehyde, 98 mg of N-(piperidin-4-yl)-2,3-dihydro-1,4-benzodioxin-6-carboxamide and 21 μl of acetic acid were added and stirred at room temperature for 2 hours. To the reaction mixture, 0.12 g of sodium triacetoxyborohydride was added and stirred at the same temperature for 30 min. Chloroform and aqueous saturated sodium hydrogen carbonate solution were added, the organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and extracts were combined, washed with aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; chloroform:methanol=20:1], and to the residue thus obtained, diethyl ether was added, and the resulting solid was filtered to give 0.12 g of N-(1-(2-(2-oxoquinoxalin-1(2H)-yl)ethyl)piperidin-4-yl)-2,3-dihydro-1,4-benzodioxin-6-carboxamide as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524738B2
Source datasetuspto-grants-2013_09
ORD IDord-7181126977fe4d56b3e830d63a85ff96
Source noteuspto-grants-2013_09