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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010322Generated: November 2, 2026

Triethylamine → N-{4-[2-(Butyroylamino)pyridin-4-yl]oxyphenyl}-N'-cyclopropylurea

https://huagongshe.com/reaction/1010322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclopropylamineHCID 69828—
ReactantPhenyl N-(4-[2-(butyroylamino)pyridin-4-yl]oxyphenyl)carbamateHCID 58931168—
SolventTetrahydrofuranHCID 8028—
ProductN-{4-[2-(Butyroylamino)pyridin-4-yl]oxyphenyl}-N'-cyclopropylureaHCID 58931404—

Reaction Steps

Phenyl N-{4-[2-(butyroylamino)pyridin-4-yl]oxyphenyl}carbamate (0.116 g), cyclopropylamine (0.034 g), triethylamine (0.041 ml) and tetrahydrofuran (10 ml) were heated together in a sealed tube at 100° C. for 1 hour. NH type silica gel was added to the reaction solution, the solvent was distilled off under reduced pressure and the reaction product was adsorbed onto the silica gel. The silica gel was charged into a dry column packed with NH type silica gel, and column purification was performed (ethyl acetate). The solvent was distilled off under reduced pressure, ethyl acetate and hexane were added to the residue, and the precipitated solid was filtered out to obtain 20 mg of the target substance as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-09097b0305e548d0af73407d1fd4095a
Source noteuspto-grants-2011_07