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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879704Generated: October 31, 2026

Benzylethanolamine → HCID 86648986, compound

https://huagongshe.com/reaction/1879704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylethanolamineHCID 4348—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86648987HCID 86648987—
SolventAcetic AcidHCID 176—
SolventAcetonitrileHCID 6342—
ProductHCID 86648986HCID 86648986101.7%

Reaction Steps

Sodium triacetoxyborohydride (1.37 g) was added to a solution of 3-chloro-5-[(3R)-3-methylmorpholin-4-yl]pyrazine-2-carbaldehyde (1.04 g), N-benzylethanolamine (0.78 g) and acetic acid (0.74 mL) in acetonitrile (20 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was basified with saturated aqueous sodium hydrogen carbonate, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over magnesium sulfate, and concentrated. The residue was purified by basic silica gel column chromatography (solvent gradient: 5→40% ethyl acetate/hexane) to give the title compound (1.65 g, quantitative) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318722B2
Source datasetuspto-grants-2012_11
ORD IDord-0baa395770ab49a3ac4b18b89cd81324
Source noteuspto-grants-2012_11