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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088950Generated: October 26, 2026

Sodium Bicarbonate → 5-Bromo-N3-[1-(tetrahydro-2H-pyran-4-yl)ethyl]pyridine-2,3-diamine

https://huagongshe.com/reaction/2088950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromopyridine-2,3-diamineHCID 691156—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-(Tetrahydro-2H-pyran-4-yl)ethanoneHCID 9877365—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product5-Bromo-N3-[1-(tetrahydro-2H-pyran-4-yl)ethyl]pyridine-2,3-diamineHCID 8665236919.6%

Reaction Steps

2,3-Diamino-5-bromopyridine (1.07 g) and 1-(tetrahydro-2H-pyran-4-yl)ethanone (0.80 g) were dissolved in methanol (20 ml), and acetic acid (0.98 ml) was added. After stirring at room temperature for a while, sodium cyanoborohydride (1.08 g) was added and the mixture was stirred at room temperature for 20 hours. A saturated aqueous sodium bicarbonate solution was added to the reaction solution, followed by extraction with ethyl acetate. Then, the organic layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The resulting residue was purified by flash column chromatography (developed with ethyl acetate-hexane) to give the title compound (334 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436012B2
Source datasetuspto-grants-2013_05
ORD IDord-a3d8a225a4414f30929277ad24c0b246
Source noteuspto-grants-2013_05