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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33472Generated: October 25, 2026

Aniline → 5-(phenylamino)-N-(2-(piperidin-1-yl)phenyl)furan-2-carboxamide

https://huagongshe.com/reaction/33472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantBinap, (A+-)-HCID 634876—
Reactant5-bromo-N-(2-piperidin-1-ylphenyl)furan-2-carboxamideHCID 889132—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTolueneHCID 1140—
Product5-(phenylamino)-N-(2-(piperidin-1-yl)phenyl)furan-2-carboxamideHCID 4444458440%

Reaction Steps

To a solution of 5-bromo-furan-2-carboxylic acid (2-piperidin-1-yl-phenyl)-amide (1.0 mmol) in toluene (7.5 mL) was added aniline (1.3 mmol), tris(dibenzylidineacetone)dipalladium(0) (“Pd2dba”) (Aldrich) (0.05 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (“BINAP”) (0.1 mmol), and potassium tert-butoxide (“t-BuOK”) (1.5 mmol), and the resulting mixture was refluxed overnight. The reaction was then cooled to room temperature, passed through a plug of silica and concentrated. Purification of the dark brown residue by HPLC afforded the product. Yield: 40%. MS: 362 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429603B2
Source datasetuspto-grants-2008_09
ORD IDord-0255c1b304a74e0d8db0f77ad6126e01
Source noteuspto-grants-2008_09