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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009753Generated: October 28, 2026

Trifluoroacetic acid → HCID 67304837, compound

https://huagongshe.com/reaction/1009753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66907494HCID 66907494—
ReactantHCID 67304799HCID 67304799—
ProductHCID 67304837HCID 6730483748%

Reaction Steps

Using an analogous procedures to those described in Example 15, 2-[4-(6-cyano-7-methoxyquinolin-4-yloxy)phenyl]acetic acid was reacted with 3-(N-tert-butoxycarbonyl-N-cyclopropylaminomethyl)-5-methylaniline and the product was reacted with trifluoroacetic acid. The resultant product was purified by column chromatography on silica using a solvent gradient from 100:0 to 9:1 mixtures of ethyl acetate and methanol as eluent. There was thus obtained the title compound in 48% yield. A portion of the material so obtained was dissolved in methylene chloride and a solution of maleic acid (1 equivalent) in ethanol was added. The resultant solution was evaporated to provide a maleate salt of the title compound which gave the following characterising data:—1H NMR: (DMSOd6) 0.73 (m, 4H), 2.3 (s, 3H), 2.64 (m, 1H), 3.72 (s, 2H), 4.07 (s, 3H), 4.11 (s, 2H), 6.01 (s, 2H), 6.52 (m, 1H), 7.0 (s, 1H), 7.3 (d, 2H), 7.35 (s, 1H), 7.5 (d, 2H), 7.62 (s, 1H), 7.66 (s, 1H), 8.76 (m, 2H), 10.26 (s, 1H); Mass Spectrum: M+H+ 493.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973164B2
Source datasetuspto-grants-2011_07
ORD IDord-a08672d204974a0ab897f1b937266c16
Source noteuspto-grants-2011_07