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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424320Generated: October 31, 2026

Triethylamine → 3-(4-{4-[(1H-benzoimidazol-2-ylamino)methyl]piperidin-1-yl}phenyl)-2-(2,4,6-trimethylbenzoylamino)propionic acid

https://huagongshe.com/reaction/1424320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(4-Boronophenyl)-2-(2,4,6-trimethylbenzoylamino)propionic acidHCID 57660948—
Reactant(1H-benzoimidazol-2-yl)piperidin-4-ylmethylamine trifluoroacetateHCID 69079613—
CatalystCupric acetateHCID 8895—
Solvent1,2-DichloroethaneHCID 11—
Product3-(4-{4-[(1H-benzoimidazol-2-ylamino)methyl]piperidin-1-yl}phenyl)-2-(2,4,6-trimethylbenzoylamino)propionic acidHCID 24872189—

Reaction Steps

95 mg (0.207 mmol, calculated as bistrifluoroacetate salt) of crude piperidine derivative (19), 113 mg (0.621 mmol) Cu(OAc)2, 147 mg (0.415 mmol) boronic acid (6) and 1.72 ml (12.42 mmol) NEt3 were mixed in 10 ml DCE and stirred at room temperature for 20 h. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in methanol and subsequently submitted to reversed phase HPLC purification using a water/acetonitrile gradient containing 0.1% TFA. The required fractions were collected and lyophilized to yield (20) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927534B2
Source datasetuspto-grants-2015_01
ORD IDord-77abbd1afe25445aa857ff55be847c6d
Source noteuspto-grants-2015_01