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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615661Generated: November 3, 2026

HCID 68089368, compound → HCID 86667815, compound

https://huagongshe.com/reaction/1615661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68089368HCID 68089368—
CatalystHCID 178418406HCID 178418406—
SolventEthanolHCID 702—
ProductHCID 86667815HCID 86667815100.9%

Reaction Steps

To a solution of [1,2,4]triazolo[1,5-h][1,7]naphthyridin-2-ylmethanol (280 mg, 1.4 mmol) in EtOH (20 mL) was added activated manganese (IV) dioxide (1.21 g, 14.0 mmol). The mixture was stirred at reflux for 2 h. Then the mixture was filtered and the filtrate was concentrated under reduce pressure to give [1,2,4]triazolo[1,5-h][1,7]naphthyridine-2-carbaldehyde as a yellow solid (280 mg, yield 88%). ESI MS: m/z 199.1 [M+H]+. 1H NMR (400 MHz, CDCl3) δ 10.34 (s, 1H), 9.16 (dd, J=1.6, 4.4 Hz, 1H), 8.55 (d, J=7.2 Hz, 1H), 8.28 (dd, J=1.6, 8.0 Hz, 1H), 7.76 (dd, J=4.4, 8.0 Hz, 1H), 7.47 (d, J=8.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765760B2
Source datasetuspto-grants-2014_07
ORD IDord-efa18ecb484049ad906c90c34a9602da
Source noteuspto-grants-2014_07