Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469800Generated: October 30, 2026

Oxalyl chloride → HCID 71294318, compound

https://huagongshe.com/reaction/469800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantAminopyrazineHCID 78747—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Cyclohexyl-6-(2,2,2-trifluoroethoxy)nicotinic acidHCID 71293952—
SolventDichloromethaneHCID 6344—
ProductHCID 71294318HCID 71294318—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 5-cyclohexyl-6-(2,2,2-trifluoro-ethoxy)-nicotinic acid (Example 4b) (50 mg, 0.16 mmol) in dichloromethane (5 mL) was added oxalylchloride (0.02 mL, 0.25 mmol) at 0° C. and the reaction mixture was stirred at 25° C. for 3 h. Solvent was removed in vacuo and the residue was dissolved in dry dichloromethane. To this was added DIPEA (0.2 mL, 0.99 mmol) followed by 2-pyrazinamine (CAN 5049-61-6, 19 mg, 0.21 mmol) at 25° C. and the reaction mixture was stirred for 12 hours at that temperature. The solvent was removed in vacuo and the crude residue was purified by prep-HPLC to give 5-cyclohexyl-N-pyrazin-2-yl-6-(2,2,2-trifluoro-ethoxy)-nicotinamide as off white solid (10 mg, 15.9%); MS (ESI): 381.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629166B2
Source datasetuspto-grants-2014_01
ORD IDord-e87c63a2661640e5acd83445459e13b2
Source noteuspto-grants-2014_01