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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710859Generated: November 2, 2026

{3-[(Cyclopentylmethyl)(ethyl)amino]-6-methoxypyridin-2-yl}methanol → 3-[(Cyclopentylmethyl)(ethyl)amino]-6-methoxypicolinaldehyde

https://huagongshe.com/reaction/1710859

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{3-[(Cyclopentylmethyl)(ethyl)amino]-6-methoxypyridin-2-yl}methanolHCID 67243028—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product3-[(Cyclopentylmethyl)(ethyl)amino]-6-methoxypicolinaldehydeHCID 8662843085%

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of {3-[(cyclopentylmethyl)(ethyl)amino]-6-methoxypyridin-2-yl}methanol (2.0 g, 7.57 mmol) in chloroform (200 mL) was added with manganese dioxide (20 g, 230 mmol), and the mixture was stirred at 55° C. for 16 hours. The reaction mixture was filtered through Celite, and the filtrate was washed with chloroform, and then concentrated under reduced pressure. The resulting residue was added with chloroform (200 mL) and manganese dioxide (20 g, 230 mmol), and the mixture was stirred at 55° C. for 6 hours. The reaction mixture was filtered through Celite, and the filtrate was washed with chloroform, and then concentrated under reduced pressure to obtain 3-[(cyclopentylmethyl)(ethyl)amino]-6-methoxypicolinaldehyde (1.68 g, 85%) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790737B2
Source datasetuspto-grants-2010_09
ORD IDord-3d96e7ef473648c4a353a7d1af2987e2
Source noteuspto-grants-2010_09