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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479794Generated: October 31, 2026

3-Aminopyridine → HCID 21904427, compound

https://huagongshe.com/reaction/479794

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminopyridineHCID 10009—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-Boc-piperidine-3-carboxaldehydeHCID 9964448—
SolventMethanolHCID 887—
SolventTrimethyl orthoformateHCID 9005—
ProductHCID 21904427HCID 2190442775.4%

Reaction Steps

To a solution of N-Boc-piperidin-3-yl-formaldehyde 3 (0.89 g, 4.16 mmol) in 3 mL of dry methanol and 3 mL of trimethylorthoformate was added 3-aminopyridine (0.39 g, 1 eq.), and the mixture was stirred at room temperature for 1.5 hours. NaBH3CN (95%, 0.29 g, 1.05 eq.) was introduced in one portion, and the mixture was stirred at room temperature overnight. The mixture was quenched with 10 mL of aqueous potassium carbonate (sat.), then extracted with ethyl acetate (3×30 mL). The extracts were combined and washed with aqueous NaHCO3 (sat., 2×10 mL), brine (20 mL), and dried over anhydrous sodium sulfate. After the solvent was removed, the remaining oily residue was purified by flash column chromatography (silica gel, hexane/ethyl acetate) to afford N-(1-Boc-piperidin-3-ylmethyl)-N-(pyridin-3-yl)amine 17 as a white solid (0.91 g, 75%). LRMS 292.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645980B1
Source datasetuspto-grants-2003_11
ORD IDord-f6bc862cbf984e73a94a8a153789dfbf
Source noteuspto-grants-2003_11