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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641136Generated: October 31, 2026

N-(4-methoxy-phenyl)-N-(tert-butyl-oxycarbonylpropyl-sulfonyl)-furo[2,3-b]quinoline-4-carboxamide → N-(4-Methoxy-phenyl)-N-(carboxypropyl-sulfonyl)-furo[2,3-b]quinoline-4-carboxamide

https://huagongshe.com/reaction/641136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-methoxy-phenyl)-N-(tert-butyl-oxycarbonylpropyl-sulfonyl)-furo[2,3-b]quinoline-4-carboxamideHCID 68637828—
SolventTrifluoroacetic acidHCID 6422—
ProductN-(4-Methoxy-phenyl)-N-(carboxypropyl-sulfonyl)-furo[2,3-b]quinoline-4-carboxamideHCID 6863797587.9%

Reaction Steps

200 mg (0.34 mmol) N-(4-Methoxy-phenyl)-N-(tert-butyl-oxycarbonylpropyl-sulfonyl)-furo[2,3-b]quinoline-4-carboxamide 9 were dissolved in 3.0 mL trifluoroacetic acid and stirred for 15 minutes at room temperature. The solvent was removed under reduced pressure to give an yellow oil. The residue was purified by silica gel chromatography (eluent: methylene chloride/diethylether 6:4+0.1% acetic acid). Evaporation of the appropriate fractions gave 140 mg of the desired product 10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07695980B2
Source datasetuspto-grants-2010_04
ORD IDord-9f5ec1e2063e4877a1c70612ee2e9431
Source noteuspto-grants-2010_04