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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243538Generated: October 30, 2026

2-Aminopyridine → Methyl 5-(pyridin-2-ylamino)pentanoate

https://huagongshe.com/reaction/1243538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantSodium BicarbonateHCID 516892—
ReactantPentanoic acid, 5-oxo-, methyl esterHCID 554053—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-(pyridin-2-ylamino)pentanoateHCID 2192781348.2%

Reaction Steps

To a solution of methyl 5-oxopentanoate (3.0 g, 23 mmol) in methylene chloride (75 mL) was added 2-aminopyridine (2.38 g, 25.3 mmol). The mixture was stirred at room temperature for 30 minutes. Then, the sodium triacetoxy borohydride (7.31 g, 34.5 mmol) was added and the mixture was stirred at room temperature for 4.5 hours. A saturated solution of sodium bicarbonate (40 mL) was added and the reaction mixture was extracted with ether (4×30 mL). The organic layer was washed with 0.1N NaOH, water (2×40 mL), dried (MgSO4) and concentrated. The residue was purified by flash chromatography 1:1 (Acetone: methylene chloride) to obtain 2.31 g (48%) of the product. 1H NMR (CDCl3) 8.09–8.06 (m, 1H), 7.42–7.38 (m, 1H), 6.59–6.52 (m, 1H), 6.37 (d, J=9 Hz, 1H), 4.52 (br s, 1H), 3.68 (s, 3H), 3.29 (q, J=6 Hz, 2H), 2.40–2.31 (m, 2H), 1.8–1.61 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119098B2
Source datasetuspto-grants-2006_10
ORD IDord-b113cb4b29f7403fb9918bdbbd896ab2
Source noteuspto-grants-2006_10