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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570610Generated: October 30, 2026

Water → 4-((1-((4-cyano-3-(trifluoromethyl)phenyl)amino)-2-methyl-1-oxopropan-2-yl)amino)-2-fluoro-N-methylbenzamide

https://huagongshe.com/reaction/570610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Amino-2-(trifluoromethyl)benzonitrileHCID 522170—
Reactant2-((3-Fluoro-4-(methylcarbamoyl)phenyl)amino)-2-methylpropanoic acidHCID 67106897—
SolventDichloromethaneHCID 6344—
Product4-((1-((4-cyano-3-(trifluoromethyl)phenyl)amino)-2-methyl-1-oxopropan-2-yl)amino)-2-fluoro-N-methylbenzamideHCID 6710679330.8%

Reaction Steps

The title compound was made in accordance with General Method 1. 2-(3-Fluoro-4-methylcarbamoyl-phenylamino)-2-methyl-propionic acid (1.27 g) was dissolved in DCM. EDC1-HCl (1.91 g) was added to it and the reaction mixture was stirred for 5 min at RT. 4-Amino-2-(trifluoromethyl)benzonitrile (1.00 g) was added portionwise and stirring was continued for 5 h at RT. Water was added to the reaction mixture, and the product was extracted with DCM. The combined organic layer was washed with water, dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by silica gel chromatography (100-200 mesh silica gel) eluting with 5% MeOH-DCM to obtain 650 mg of 4-[1-(4-Cyano-3-trifluoromethyl-phenylcarbamoyl)-1-methyl-ethylamino]-2-fluoro-N-methyl-benzamide, HPLC, Column: YMC ODS AQ, 4.6×250 mm, 5 μm, Mobile Phase A: 0.05% TFA, Mobile Phase B: ACN, Gradient: 10% to 90% B in 10 min, hold for 10 min, 90% to 10% B in 1 min, Flow Rate: 1 mL/min, Retention time: 11.174 min, M+1: 423.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023869B2
Source datasetuspto-grants-2015_05
ORD IDord-571fd10451b54f5998fc5c046bb0ba28
Source noteuspto-grants-2015_05