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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240062Generated: October 25, 2026

Diisopropylethylamine → 8-Trifluoromethoxy-2-oxo-2H-chromene-3-carboxylic acid (2',4'-dimethoxy-biphenyl-3-yl)-amide

https://huagongshe.com/reaction/240062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(2,4-Dimethoxyphenyl)anilineHCID 2758411—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant8-Trifluoromethoxy-3-carboxy-coumarinHCID 86650358—
SolventDimethylformamideHCID 6228—
Product8-Trifluoromethoxy-2-oxo-2H-chromene-3-carboxylic acid (2',4'-dimethoxy-biphenyl-3-yl)-amideHCID 8665037570%

Reaction Steps

DIEA (0.013 mL, 0.072 mmol) was added to 8-trifluoromethoxy-3-carboxy-coumarin (0.018 g, 0.065 mmol) and HATU (0.027 g, 0.072 mmol) in 0.36 mL of DMF with constant stirring at room temperature until a clear solution resulted. Subsequently, 2′,4′-dimethoxy-biphenyl-3-ylamine (0.015 g, 0.065 mmol) was added and allowed to react overnight. DMF was removed under vacuum and the reaction was resuspended in DMSO. The crude product was purified on a Parallex Flex parallel preparative reverse phase HPLC instrument (Biotage) using a solvent gradient of 10-95% ACN/H2O with 0.05% TFA at a flow rate of 20 mL/min. UV absorbance was monitored at 254 nm and the fractions corresponding to the product peak were collected and the solvent removed under vacuum to give 0.022 g of product in 70% yield: LCMS (ESI) m/z 486 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642788B2
Source datasetuspto-grants-2014_02
ORD IDord-2d04cd493c9542bf8b8e6d6093304dd5
Source noteuspto-grants-2014_02