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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78178Generated: October 28, 2026

(2-Amino-6-methylpyridin-3-yl)methanol → 2-Amino-6-methylnicotinaldehyde

https://huagongshe.com/reaction/78178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Amino-6-methylpyridin-3-yl)methanolHCID 55281422—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product2-Amino-6-methylnicotinaldehydeHCID 5340103088%

Reaction Steps

To a methylene chloride (8 mL) solution of (2-amino-6-methyl-pyridin-3-yl)-methanol (379 mg, 2.74 mmol) described in Manufacturing Example 170-1-3 was added manganese (IV) dioxide (1.19 mg, 13.7 mmol) at room temperature, which was stirred for 11 hours at room temperature. The reaction mixture was filtered through a Celite pad, and the filtrate was concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=1:2) to obtain the title compound (328 mg, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-a60202206eff4d63ab42a3c601ba83ed
Source noteuspto-grants-2014_09