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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066204Generated: November 3, 2026

Triethylamine → HCID 59596894, compound

https://huagongshe.com/reaction/2066204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant1-[(4-Fluorophenyl)carbamoyl]cyclopropanecarboxylic AcidHCID 21081530—
ReactantHCID 23153096HCID 23153096—
SolventDimethylformamideHCID 6228—
ProductHCID 59596894HCID 5959689430%

Reaction Steps

4-(Dimethylaminomethyl)piperidine-1-carboxylic acid [4-(4-amino-2-fluorophenoxy)pyridin-2-yl]amide (88 mg) was dissolved in N,N-dimethylformamide (2.5 ml). 1-(4-Fluorophenylcarbamoyl)cyclopropanecarboxylic acid (101 mg), triethylamine (0.0633 ml) and benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (201 mg) were added under a nitrogen atmosphere at room temperature, followed by stirring overnight. Liquid-liquid separation was carried out after addition of ethyl acetate and water to the reaction mixture. The organic layer was washed with a 1N aqueous solution of sodium hydroxide and brine, and dried over anhydrous sodium sulfate. The solvent was removed and the resultant residue was purified by silica gel column chromatography (Fuji Silysia NH, eluent; ethyl acetate, then ethyl acetate:methanol=98:2). Fractions containing the target compound were concentrated under reduced pressure. A solid was precipitated by addition of heptane to the resultant residue. The solid was collected by filtration, and dried under aeration to provide the titled compound as white powder (39.8 mg, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288538B2
Source datasetuspto-grants-2012_10
ORD IDord-9dd112b7c3eb4ce58f8c9caa7f056e04
Source noteuspto-grants-2012_10