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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487404Generated: October 29, 2026

HCID 19093752, compound → HCID 19093708, compound

https://huagongshe.com/reaction/487404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19093752HCID 19093752—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 19093708HCID 1909370877.1%

Reaction Steps

A solution of N-tert-butyl-4'-[(5,7-diethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-1-yl)methyl]biphenyl-2-sulphonamide (200 mg) in trifluoroacetic acid (5 ml) was heated at reflux for 3 hours. Volatile material was removed by evaporation and water was added to the residue. The resultant solution was basified by the addition of solid potassium carbonate and then extracted twice with ethyl acetate. The combined extracts were washed with water, saturated sodium chloride solution and then dried (MgSO4). The solvent was removed by evaporation to give 4'-[(5,7-diethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-1-yl)methyl]biphenyl-2-sulphonamide as a solid (137 mg); m.p. 199°-200° C.; NMR (d6 -DMSO): 1.18(t, 3H), 1.26(t, 3H), 2.73(q, 2H), 3.07(q, 2H), 5.54(s, 2H), 6.72(d, 1H), 7.1-7.7(m, 10H), 8.01(dd, 1H), 8.23(d, 1H); mass spectrum (+ve FAB, methanol/NBA): 448 (M+H)+ ; microanalysis, found: C, 67.0; H, 5.5; N, 9.2%; C25H25N3O3S requires: C, 67.1; H, 5.6; N, 9.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05294620
Source datasetuspto-grants-1994_03
ORD IDord-ab66f4aa0ec64ea1af67dffeace2d79f
Source noteuspto-grants-1994_03