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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17151Generated: October 28, 2026

(4-Amino-3-bromothieno[3,2-c]pyridin-7-yl)methanol → 4-Amino-3-bromothieno[3,2-c]pyridine-7-carbaldehyde

https://huagongshe.com/reaction/17151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Amino-3-bromothieno[3,2-c]pyridin-7-yl)methanolHCID 18450834—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-3-bromothieno[3,2-c]pyridine-7-carbaldehydeHCID 1845083589%

Reaction Steps

A solution of Example 277E (1 g, 3.86 mmol) in THF (100 mL) was treated with MnO2 (2.66 g, 42.1 mmol), stirred overnight at room temperature, and filtered through diatomaceous earth (Celite®). The pad was washed with THF and dichloromethane and the combined filtrates were concentrated to provide 0.88 g (89% yield) of the desired product. MS (ESI(+)) m/e 256.8, 258.8 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737160B2
Source datasetuspto-grants-2010_06
ORD IDord-fabe84145ad840b4b3c077c5acb259a2
Source noteuspto-grants-2010_06