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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270875Generated: November 1, 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/1270875

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 numberUS07202363B2
Source datasetuspto-grants-2007_04
ORD IDord-14f850998a1c461aaed73be7ff0a9a74
Source noteuspto-grants-2007_04