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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201533Generated: October 29, 2026

Hydrochloric Acid → HCID 117771050, compound

https://huagongshe.com/reaction/2201533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 117771043HCID 117771043—
SolventDimethylformamideHCID 6228—
ProductHCID 117771050HCID 11777105064.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirring solution of 6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)-N-((5-fluoropyridin-2-yl)methyl)-3-methoxypicolinamide (40 mg, 0.05 mmol) in DMF (5 mL) was added Py.HCl (400 mg, 2.22 mmol) under N2 protection. The mixture was stirred in a pre-heated oil-bath at 100° C. for 10 h. The mixture was concentrated in vacuo, diluted with water and extracted with EtOAc. After being washed with brine, dried over Na2SO4, filtered and evaporated, the crude product was purified by prep-TLC (PE:EtOAc=2:1) to give the product of 6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)-N-((5-fluoropyridin-2-yl)methyl)-3-hydroxypicolinamide (20 mg, yield: 58%). 1H-NMR (CDCl3, 400 MHz) δ 12.14 (s, 1H), 8.91 (d, J=5.6 Hz, 1H), 8.33 (s, 1H), 7.94 (s, 1H), 7.86˜7.89 (m, 2H), 7.60 (d, J=8.8 Hz, 1H), 7.52 (s, 1H), 7.36 (d, J=8.8 Hz, 1H), 7.31˜7.33 (m, 2H), 7.15 (d, J=8.8 Hz, 2H), 5.78 (d, J=4.0 Hz, 1H), 4.68 (d, J=5.6 Hz, 2H), 3.12 (s, 3H), 2.92 (d, J=4.8 Hz, 3H), 2.76 (s, 3H). MS (M+H)+: 622.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364482B2
Source datasetuspto-grants-2016_06
ORD IDord-c6ec3cea2d334802b8eee33bc6e49ab2
Source noteuspto-grants-2016_06