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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710857Generated: November 2, 2026

Water → N-(cyclopentylmethyl)-N-ethyl-6-methoxy-2-[(methoxymethoxy)methyl]pyridin-3-amine

https://huagongshe.com/reaction/1710857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyclopentanecarbaldehydeHCID 70106—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-Ethylamino-6-methoxy-2-(methoxymethyloxy)methylpyridineHCID 67242334—
Solvent1,2-DichloroethaneHCID 11—
ProductN-(cyclopentylmethyl)-N-ethyl-6-methoxy-2-[(methoxymethoxy)methyl]pyridin-3-amineHCID 6724295286%

Reaction Steps

A solution of N-ethyl-6-methoxy-2-[(methoxymethoxy)methyl]pyridin-3-amine (7.20 g, 31.8 mmol) and cyclopentanecarbaldehyde (3.75 g, 38.2 mmol) in 1,2-dichloroethane (240 mL) was added with sodium triacetoxyborohydride (8.75 g, 41.3 mmol), and the mixture was stirred at room temperature for 12 hours. The reaction mixture was added with water, and extracted with chloroform. The organic layers were combined, washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=8:1) to obtain N-(cyclopentylmethyl)-N-ethyl-6-methoxy-2-[(methoxymethoxy)methyl]pyridin-3-amine (8.39 g, 86%) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790737B2
Source datasetuspto-grants-2010_09
ORD IDord-c7ac2f3d88d843fa81ac25dc6f7e2bda
Source noteuspto-grants-2010_09