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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552408Generated: October 31, 2026

m-Anisoyl chloride → HCID 58024296, compound

https://huagongshe.com/reaction/552408

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Anisoyl chlorideHCID 74374—
Reactant7-(3-aminophenoxy)-1H-imidazo[4,5-b]pyridin-2(3H)-oneHCID 45140141—
ProductHCID 58024296HCID 5802429640%

Reaction Steps

Method H was used with 7-(3-aminophenoxy)-1H-imidazo[4,5-b]pyridin-2(3H)-one and 3-methoxy-benzoyl chloride to afford the title compound as a brown solid (21 mg, 40%). 1H-NMR (δ, ppm, DMSO-d6): 3.83 (s, 3H, OMe), 6.49 (d, 1H, HPy,5, J=5.8 Hz), 6.90 (d, 1H, Harom, J=7.48 Hz), 7.16 (d, 1H, Harom, J=6.52 Hz), 7.39-7.49 (m, 3H, Harom), 7.52 (d, 1H, Harom, J=7.61 Hz), 7.62-7.68 (m, 2H, Harom), 7.81 (d, 1H, HPy,6, J=5.44 Hz), 10.31 (s, 1H, NHamide), 11.19 (s, 1H, NHPy3), 11.39 (s, 1H, NHPy2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951819B2
Source datasetuspto-grants-2011_05
ORD IDord-d4814be2465d4e648aa476cb94f7931e
Source noteuspto-grants-2011_05