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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791357Generated: October 27, 2026

Triethylamine → Methyl 1-(pyridin-2-ylmethyl)piperidine-2-carboxylate

https://huagongshe.com/reaction/1791357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
Reactant2-PyridinecarboxaldehydeHCID 14273—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl Pipecolinate HydrochlorideHCID 13246231—
Solvent1,1-DichloroethaneHCID 6365—
ProductMethyl 1-(pyridin-2-ylmethyl)piperidine-2-carboxylateHCID 1177620693.6%

Reaction Steps

Methyl pipecolinate hydrochloride (9.0 g, 50 mmol) was mixed with pyridine-2-carbaldehyde (5.4 g, 50 mmol) and triethylamine (5.05 g, 50 mmol) in dichloroethane (180 mL) at room temperature. Sodium triacetoxyborohydride (14.8 g, 70 mmol) was added in one portion. After the reaction mixture was stirred at room temperature for 1.5 h, saturated sodium carbonate was added. Then the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried with sodium sulfate, filtered and concentrated to give 10.9 g (93.6%) of the title compound as a pale brown oil. 1H NMR (CDCl3), δ(ppm): 8.53 (d, 1H), 7.65 (td, 1H), 7.49 (d, 1H), 7.14 (t, 1H), 3.89 (d, 1H), 3.73 (s, 3H), 3.68 (d, 1H), 3.25 (dd, 1H), 2.97 (m, 1H), 2.25 (m, 1H), 1.85 (m, 2H), 1.30-1.76(m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074809B2
Source datasetuspto-grants-2006_07
ORD IDord-c969145559604c7d8937ea3bf6a22d15
Source noteuspto-grants-2006_07