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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201547Generated: October 28, 2026

HCID 117771438, compound → HCID 117771656, compound

https://huagongshe.com/reaction/2201547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 117771438HCID 117771438—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 117771656HCID 11777165670%

Reaction Steps

To a solution of 3-(benzyloxy)-N-(4-fluorobenzyl)-6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)picolinamide (361 mg, 0.51 mmol) in CH3OH (5 mL) was added Pd—C under Ar. The suspension was degassed under vacuum and purged with H2 several times. The mixture was stirred under H2 at RT overnight. After being filtered through celite and removal of the solvent by concentration, the residue was purified by prep-TLC (DCM:MeOH=60:1) to afford the product of N-(4-fluorobenzyl)-6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)-3-hydroxypicolinamide. (220 mg, yield: 70%). 1H-NMR (CDCl3, 400 MHz) δ 12.27 (s, 1H), 8.61˜8.64 (m, 1H), 7.91˜7.96 (m, 3H), 7.64 (d, J=8.8 Hz, 1H), 7.55 (s, 1H), 7.42 (d, J=8.4 Hz, 1H), 7.35 (dd, J=5.6, 8.4 Hz, 2H), 7.21 (t, J=8.4 Hz, 2H), 7.01 (t, J=8.4 Hz, 2H), 5.80 (d, J=3.6 Hz, 1H), 4.59 (d, J=6.4 Hz, 2H), 3.04 (s, 3H), 2.97 (d, J=5.2 Hz, 3H), 2.91 (s, 3H). MS (M+H)+: 621.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364482B2
Source datasetuspto-grants-2016_06
ORD IDord-a9f1e7631aab4f94ab2a84819681d007
Source noteuspto-grants-2016_06