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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201518Generated: October 29, 2026

HCID 117771342, compound → HCID 117771752, compound

https://huagongshe.com/reaction/2201518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 117771342HCID 117771342—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 117771752HCID 11777175271.8%

Reaction Steps

A mixture of N-benzyl-3-(benzyloxy)-6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)picolinamide (200 mg, 0.29 mmol) and Pd/C (10 mg) in CH3OH (10 mL) was stirred at room temperature overnight under H2 atmosphere (50 psi). The mixture was filtered and the filtrate was concentrated in vacuum. The residue was purified by prep-TLC (DCM:EtOAc=5:1) to give the product of N-benzyl-6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)-3-hydroxypicolinamide (125 mg, yield: 71.8%). 1H-NMR (CDCl3, 400 MHz) δ 8.73 (br s, 1H), 7.84˜7.87 (m, 3H), 7.63 (d, J=8.4 Hz, 1H), 7.49 (s, 1H), 7.44 (d, J=8.4 Hz, 1H), 7.30˜7.36 (m, 4H), 7.26 (d, J=6.0 Hz, 1H), 7.19 (t, J=8.0 Hz, 2H), 6.39 (br s, 1H), 4.60 (d, J=4.8 Hz, 2H), 3.04 (s, 3H), 2.93 (d, J=3.2 Hz, 3H), 2.87 (s, 3H). MS (M+H)+: 603.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364482B2
Source datasetuspto-grants-2016_06
ORD IDord-ac3cabca1db14411b6fd5743e0c68096
Source noteuspto-grants-2016_06