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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768192Generated: October 25, 2026

Acetic Acid → Ethyl 4-[(4-[(tert-butoxycarbonyl)amino]pyridin-3-yl methyl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1768192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,1-DichloroethaneHCID 6365—
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-Boc4-amino-3-pyridine carboxaldehydeHCID 20848820—
ProductEthyl 4-[(4-[(tert-butoxycarbonyl)amino]pyridin-3-yl methyl)amino]piperidine-1-carboxylateHCID 22293255—

Reaction Steps

Sodium triacetoxyborohydride (1.70 g, 8.03 mmol) and acetic acid (0.29, 4.82 mmol) were added to a solution of N-Boc-4-amino-3-pyridine carboxaldehyde (0.36 g, 1.61 mmol) and ethyl 4-aminopiperidine-1-carboxylate (0.33 g, 1.93 mmol) in dichloroethane (5 mL) at room temperature. The reaction was stirred overnight, and quenched with saturated aqueous sodium bicarbonate. This was separated, extracted with ethyl acetate and the combined organics were dried over sodium sulfate. The solution was filtered and evaporated to give the crude product. This was purified by chromatography (silica gel, 0 to 12% methanol in methylene chloride gradient elution), which gave the title compound (0.24 g). MS 379.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235545B2
Source datasetuspto-grants-2007_06
ORD IDord-5ce57c3cda794f038f311fa3e1e48b39
Source noteuspto-grants-2007_06