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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072243Generated: October 26, 2026

1-(Pyridin-3-yl)ethan-1-amine → (6,4'-Dimethoxy-biphenyl-3-ylmethyl)-(1-pyridin-3-yl-ethyl)amine

https://huagongshe.com/reaction/1072243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Pyridin-3-yl)ethan-1-amineHCID 2771688—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant6,4'-Dimethoxybiphenyl-3-carbaldehydeHCID 22391191—
Solvent1,1-DichloroethaneHCID 6365—
Product(6,4'-Dimethoxy-biphenyl-3-ylmethyl)-(1-pyridin-3-yl-ethyl)amineHCID 2239132350%

Reaction Steps

1-Pyridin-3-yl-ethylamine (245 mg, 2 mmol) and 6,4′-Dimethoxy-biphenyl-3-carbaldehyde (121 mg, 0.5 mmol) were dissolved in dichloroethane (10 mL). After stirring for 6 h at room temperature, the sodium triacetoxyborohydride (212 mg, 1.0 mmol, Aldrich) was added to the solution at 0 C. The mixture was stirred under nitrogen at room temperature for overnight then the reaction was cooled at ice bath and quenched with saturated aqueous sodium bicarbonate (10 mL). The organic phase was separated and the aqueous phase was extracted with dichloroethane (10 mL×3). The combined organic layers were dried over anhydrous magnesium sulfate and concentrated via vacuo. The crude was purified by column chromatography (silica gel, ethyl acetate) to give the title compound as white solid in 50% yield (87 mg, 0.25 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908935B2
Source datasetuspto-grants-2005_06
ORD IDord-2d4e5b8ae6de4dc088c819a6297f8c2d
Source noteuspto-grants-2005_06