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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240090Generated: October 31, 2026

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

https://huagongshe.com/reaction/240090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-[2-(Trifluoromethoxy)phenyl]anilineHCID 16768736—
Reactant8-Trifluoromethoxy-3-carboxy-coumarinHCID 86650358—
SolventDimethylformamideHCID 6228—
Product8-Trifluoromethoxy-2-oxo-2H-chromene-3-carboxylic acid (2'-trifluoromethoxy-biphenyl-3-yl)-amideHCID 8665039690%

Reaction Steps

DIEA (0.011 mL, 0.065 mmol) was added to 8-trifluoromethoxy-3-carboxy-coumarin (0.016 g, 0.059 mmol) and HATU (0.025 g, 0.065 mmol) in 0.36 mL of DMF with constant stirring at room temperature until a clear solution resulted. Subsequently, 2′-trifluoromethoxy-biphenyl-3-ylamine (0.015 g, 0.059 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 were collected and the solvent removed under vacuum to give 0.027 g of product in 90% yield: LCMS (ESI) m/z 510 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642788B2
Source datasetuspto-grants-2014_02
ORD IDord-b80e82f3a11e4068a1cb3360d5d86f6f
Source noteuspto-grants-2014_02