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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(Pyridin-3-yl)ethan-1-amine | HCID 2771688 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 6,4'-Dimethoxybiphenyl-3-carbaldehyde | HCID 22391191 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | (6,4'-Dimethoxy-biphenyl-3-ylmethyl)-(1-pyridin-3-yl-ethyl)amine | HCID 22391323 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06908935B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-2d4e5b8ae6de4dc088c819a6297f8c2d |
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| Source note | uspto-grants-2005_06 |
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