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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504504Generated: November 1, 2026

HCID 117737203, compound → HCID 117737243, compound

https://huagongshe.com/reaction/1504504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 117737203HCID 117737203—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 117737243HCID 1177372431.64%

Reaction Steps

1-(5-Fluoro-2-methoxy-4-(4-methyl-2-oxopyridin-1(2H)-yl)phenyl)-N-(isoxazol-3-yl)-N-(4-methoxybenzyl)-2-oxo-1,2-dihydroquinoline-6-sulfonamide (18 mg, 0.028 mmol) was taken up in TFA (2 mL) in a microwave vial and irradiated to 70° C. for 1 h. Concentration under a stream of N2 followed by column chromatography (5 g Redisep gold column, 0-80% [3:1 EtOAc/EtOH]/hept gradient with 10% DCM) afforded 1-(5-fluoro-2-methoxy-4-(4-methyl-2-oxo-1(2H)-pyridinyl)phenyl)-N-3-isoxazolyl-2-oxo-1,2-dihydro-6-quinolinesulfonamide (0.24 mg, 0.459 μmol, 1.640% yield) as a colorless residue. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 2.55 (s, 3 H) 3.72 (s, 3 H) 6.64 (d, J=1.76 Hz, 1 H) 6.88 (d, J=9.74 Hz, 1 H) 6.98-7.02 (m, 2 H) 7.11 (d, J=6.84 Hz, 1 H) 7.32 (d, J=1.35 Hz, 2H) 7.80-7.90 (m, 2 H) 8.15 (d, J=2.07 Hz, 1 H) 8.23 (d, J=5.39 Hz, 1 H) 8.29 (d, J=1.66 Hz, 1 H). m/z (ESI) 523.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212182B2
Source datasetuspto-grants-2015_12
ORD IDord-17e24f84017640d3867ccca73b99c3ff
Source noteuspto-grants-2015_12