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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930313Generated: October 29, 2026

Oxalyl chloride → HCID 86732140, compound

https://huagongshe.com/reaction/930313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Cyano-3-methylpyridine-2-carboxylic acidHCID 66665846—
ReactantHCID 86732135HCID 86732135—
ReactantHCID 86732141HCID 86732141—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86732140HCID 8673214048%

Reaction Steps

To a solution of 5-cyano-3-methylpicolinic acid (intermediate 16, 0.050 g, 0.308 mmol) in DCM (2.5 mL) was added oxalyl chloride (0.040 mL, 0.463 mmol) and a drop of DMF. The reaction mixture was stirred for 30 min at room temperature. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in DCM (1 mL). A flask was charged with a solution of tert-butyl ((4S,6S)-4-(6-amino-3-fluoropyridin-2-yl)-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-yl)carbamate (7k, 0.080 g, 0.204 mmol) and N,N-diisopropylethylamine (0.142 mL, 0.816 mmol, Aldrich) in DCM (2 mL). The solution of 5-cyano-3-methylpicolinoyl chloride was added and the reaction mixture was stirred at room temperature for 30 min, diluted with aqueous saturated NaHCO3 solution and extracted with EtOAc. The organic extract was washed with brine and dried over Na2SO4. The solution was concentrated under reduced pressure. The crude material was purified by silica gel chromatography (gradient of 5-50% EtOAc in hexane) to afford the title compound as a white solid (52 mg, 48% yield). MS m/z=537 [M+H]+. Calculated for C24H24F4N6O4: 536.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-103681221a1e403fb59450e37ac79cf4
Source noteuspto-grants-2016_03