Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422622Generated: October 31, 2026

Diisopropylethylamine → 4-{[(3-Chloro-pyrazin-2-yl)-(2-phenyl-quinolin-7-yl)-methyl]carbamoyl}-piperidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/422622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl 4-(chlorocarbonyl)piperidine-1-carboxylateHCID 2776270—
Reactant(3-Chloropyrazin-2-yl)(2-phenylquinolin-7-yl)methanamineHCID 51051365—
SolventDichloromethaneHCID 6344—
Product4-{[(3-Chloro-pyrazin-2-yl)-(2-phenyl-quinolin-7-yl)-methyl]carbamoyl}-piperidine-1-carboxylic acid benzyl esterHCID 57681029—

Reaction Steps

A CH2Cl2 solution (111.0 mL) of C-(3-chloro-pyrazin-2-yl)-C-(2-phenyl-quinolin-7-yl)-methylamine (1.9 g, 5.5 mmol) and PS-DIPEA (2.8 g, 11.1 mmol) in a round bottom flask under N2 atmosphere was charged with 4-chlorocarbonyl-piperidine-1-carboxylic acid benzyl ester (1.4 g, 5.0 mmol) and stirred at rt for 1.5 h. The reaction mixture was filtered and concentrated in vacuo. The resulting residue was purified by silica gel chromatography (Jones Flashmaster, 20 g/70 mL cartridge, eluting with 100% CH2Cl2 to 10% CH3CN/CH2Cl2) to afford 4-{[(3-chloro-pyrazin-2-yl)-(2-phenyl-quinolin-7-yl)-methyl]-carbamoyl}-piperidine-1-carboxylic acid benzyl ester as a pale yellow solid; MS (ES+): m/z 592/594 (100/50) [MH+]; HPLC: tR=3.7 min (OpenLynx, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101613B2
Source datasetuspto-grants-2012_01
ORD IDord-7bccf7a28315477ca7df3c9ebfaa01b8
Source noteuspto-grants-2012_01