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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452979Generated: October 30, 2026

(2-(Sec-butylamino)thiazolo[5,4-b]pyridin-5-yl)methanol → 2-(Sec-butylamino)thiazolo[5,4-b]pyridine-5-carbaldehyde

https://huagongshe.com/reaction/1452979

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-(Sec-butylamino)thiazolo[5,4-b]pyridin-5-yl)methanolHCID 86257065—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
Product2-(Sec-butylamino)thiazolo[5,4-b]pyridine-5-carbaldehydeHCID 57527242—

Reaction Steps

To a solution of (2-(sec-butylamino)thiazolo[5,4-b]pyridin-5-yl)methanol (0.1155 g, 0.487 mmol, 1.0 eq.) in THF (3.5 mL) under nitrogen was added MnO2 (0.6357 g, 7.3 mmol, 15.0 eq.). After 1 hr, the reaction solution was filtered through Celite and rinsed with THF. The filtrate was concentrated in vacuo to give crude 2-(sec-butylamino)thiazolo[5,4-b]pyridine-5-carbaldehyde as a colorless oil which was carried to the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473784B2
Source datasetuspto-grants-2009_01
ORD IDord-43e49d607ffc4316b9911cfe20d6bbd2
Source noteuspto-grants-2009_01