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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594293Generated: October 30, 2026

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

https://huagongshe.com/reaction/594293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-(4-Methylthiazol-2-yl)pyridin-4-yl)methanolHCID 69083230—
CatalystManganese dioxideHCID 14801—
Solvent1,2-DichloroethaneHCID 11—
Product2-(4-Methylthiazol-2-yl)isonicotinaldehydeHCID 86695619—

Reaction Steps

A solution of (2-(4-methylthiazol-2-yl)pyridin-4-yl)methanol (750 mg; 3.64 mmol) in anh. DCE (40 ml) was treated with MnO2 (1.581 g; 18.20 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-(4-methylthiazol-2-yl)isonicotinaldehyde as an off-white solid. LC-MS (conditions A): tR=0.64 min.; [M+H]+: 205.04 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-984b2cad35f944ea8766820f9c0eb8f0
Source noteuspto-grants-2016_01