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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971025Generated: October 25, 2026

Hydrogen Peroxide → 8-Fluoro-1-[(2,4,6-trifluorophenyl)amino]-5H-pyrido[4,3-b]indole-4-carboxamide

https://huagongshe.com/reaction/1971025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
Reactant8-Fluoro-1-[(2,4,6-trifluorophenyl)amino]-5H-pyrido[4,3-b]indole-4-carbonitrileHCID 59543157—
SolventDimethyl SulfoxideHCID 679—
Product8-Fluoro-1-[(2,4,6-trifluorophenyl)amino]-5H-pyrido[4,3-b]indole-4-carboxamideHCID 42636080—

Reaction Conditions

Temperature70 °C

Reaction Steps

8-Fluoro-1-[(2,4,6-trifluorophenyl)amino]-5H-pyrido[4,3-b]indole-4-carbonitrile (46.5 mg, 0.13 mmol) and K2CO3 (108 mg, 0.78 mmol) was dissolved in DMSO (2.6 ml). Hydrogen peroxide (30%, 0.100 ml, 1.04 mmol) was added and the solution was heated at 70° C. for three hours. HPLC/MS then showed complete conversion. The solution was cooled to ambient temperature and directly purified by reverse phase HPLC. Desired fractions were combined, diluted with ethyl acetate, and washed with saturated aqueous sodium bicarbonate solution: The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo to afford the title compound. 1H NMR (600 MHz, CD30OD) δ 8.37 (s, 1H); 8.16 (dd, 1H); 7.64 (dd, 1H); 7.21 (dt, 1H); 6.98 (dd, 2H). LRMS (APCI) calc'd for (C18H10F4N4O) [M+H]+, 375.1. found 375.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431569B2
Source datasetuspto-grants-2013_04
ORD IDord-ba86b3e25705455f9f134ec8e7aa037e
Source noteuspto-grants-2013_04