HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988769Generated: November 1, 2026
3-Aminopyridine → HCID 21904427, compound
https://huagongshe.com/reaction/988769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-Boc-piperidine-3-carboxaldehyde | HCID 9964448 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Trimethyl orthoformate | HCID 9005 | — |
| Product | HCID 21904427 | HCID 21904427 | 75.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06635661B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-3c191b2823c547c8851e2a20255aed66 |
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| Source note | uspto-grants-2003_10 |
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