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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390646Generated: October 31, 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/2390646

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 numberUS08273736B2
Source datasetuspto-grants-2012_09
ORD IDord-95817262f5d6454d9c1bff2d3a539ff1
Source noteuspto-grants-2012_09