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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214075Generated: November 1, 2026

Pyridine → HCID 10093668, compound

https://huagongshe.com/reaction/2214075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
ReactantAminopyrazineHCID 78747—
Reactant(2R)-2-[3-Chloro-4-(methanesulfonyl)phenyl]-3-(2-oxocyclopentyl)propanoic acidHCID 21051846—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10093668HCID 1009366851.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2(R)-(3-chloro-4-methanesulfonyl-phenyl)-3-(2-oxo-cyclopentyl)-propionic acid (125 mg, 0.36 mmol) in methylene chloride (3.62 mL) cooled to 0° C. was treated with a 2.0M solution of oxalyl chloride in methylene chloride (0.20 mL, 0.39 mmol) and a few drops of N,N-dimethylformamide. The reaction mixture was stirred at 0° C. for 10 min and at 25° C. for 20 min. The reaction mixture was then treated with a solution of 2-aminopyrazine (76 mg, 0.80 mmol) and pyridine (0.06 mL, 0.80 mmol) in tetrahydrofuran (1.81 mL). This solution was stirred at 25° C. for 1 h. At this time, the reaction was concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230–400 mesh, 75/25 ethyl acetate/hexanes) afforded 2(R)-(3-chloro-4-methanesulfonyl-phenyl)-3-(2-oxo-cyclopentyl)-N-pyrazin-2-yl-propionamide (77.6 mg, 50.7%) as a white foam: EI-HRMS m/e calcd for C19H20ClN3O4S (M+) 421.0863, found 421.0868.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105671B2
Source datasetuspto-grants-2006_09
ORD IDord-ae4e352fa82840f696c1225147804054
Source noteuspto-grants-2006_09