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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77849Generated: October 28, 2026

(2-Amino-6-methoxymethyl-pyridin-3-yl)methanol → 2-Amino-6-methoxymethyl-pyridine-3-carbaldehyde

https://huagongshe.com/reaction/77849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Amino-6-methoxymethyl-pyridin-3-yl)methanolHCID 59255403—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product2-Amino-6-methoxymethyl-pyridine-3-carbaldehydeHCID 5925546384.2%

Reaction Steps

To a mixture of (2-amino-6-methoxymethyl-pyridin-3-yl)methanol (260 mg, 1.5 mmol) described in Manufacturing Example 26-1-5 and methylene chloride (15 mL) was added manganese dioxide (1.3 g, 15 mmol), which was stirred overnight 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 (ethyl acetate:heptane=3:2) to obtain the title compound (210 mg, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-87b167fddd2b4821876c27ca7101c46b
Source noteuspto-grants-2014_09