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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594296Generated: October 31, 2026

(2-(5-Methylthiazol-2-yl)pyridin-4-yl)methanol → 2-(5-Methylthiazol-2-yl)isonicotinaldehyde

https://huagongshe.com/reaction/594296

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-(5-Methylthiazol-2-yl)pyridin-4-yl)methanolHCID 69084104—
CatalystManganese dioxideHCID 14801—
Solvent1,2-DichloroethaneHCID 11—
Product2-(5-Methylthiazol-2-yl)isonicotinaldehydeHCID 86695620—

Reaction Steps

A solution of (2-(5-methylthiazol-2-yl)pyridin-4-yl)methanol (1.910 g; 9.26 mmol) in anh. DCE (80 ml) was treated with MnO2 (4.025 g; 46.30 mmol), and the resulting mixture was heated at reflux, under nitrogen, for 1.5 h. After cooling to rt, the resulting reaction mixture was filtered over celite, and the separated solids were washed with DCM. The filtrate was concentrated to dryness under reduced pressure giving 2-(5-methylthiazol-2-yl)isonicotinaldehyde as an off-white solid. LC-MS (conditions A): tR=0.65 min.; [M+H]+: 205.35 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-b54819fc474c4e8cace0e9fd001506fd
Source noteuspto-grants-2016_01