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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023368Generated: November 1, 2026

Diethyl Pyrocarbonate → HCID 53361738, compound

https://huagongshe.com/reaction/1023368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl PyrocarbonateHCID 3051—
ReactantTriethylamineHCID 8471—
ReactantHCID 67327057HCID 67327057—
ReactantHCID 67328153HCID 67328153—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 53361738HCID 53361738—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (E)-3-{3-chloro-5-methyl-4-[(5-{[4-(trifluoromethyl)benzyl]-oxy}pyridin-2-yl)oxy]phenyl}prop-2-enoic acid (139 mg) and 4-{2-[4-(piperazin-1-ylmethyl)-phenyl]ethoxy}benzonitrile trifluoroacetate (131 mg) in DMF (6 mL) was added DEPC (0.073 mL) and Et3N (0.165 mL) at 0° C. After stirring at 0° C. for 1 hour, to the reaction mixture was added H2O, and extracted with AcOEt. The organic layer was washed with saturated aqueous NaCl, dried over anhydrous MgSO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (AcOEt) to give 4-{2-[4-({4-[(E)-3-{3-chloro-5-methyl-4-[(5-{[4-(trifluoromethyl)benzyl]oxy}pyridin-2-yl)oxy]phenyl}prop-2-enoyl]piperazin-1-yl}methyl)phenyl]ethoxy}benzonitrile as a pale yellow amorphous (195 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722663B2
Source datasetuspto-grants-2014_05
ORD IDord-4be07b9779d742d69c09405ad6250982
Source noteuspto-grants-2014_05