Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930396Generated: October 28, 2026

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride → HCID 86732229, compound

https://huagongshe.com/reaction/930396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
Reactant5-Cyanopyridine-2-carboxylic acidHCID 12400734—
ReactantHCID 86732228HCID 86732228—
SolventMethanolHCID 887—
ProductHCID 86732229HCID 8673222936.9%

Reaction Steps

To a cooled (ice bath) solution of 5-cyanopicolinic acid (0.043 g, 0.293 mmol) in MeOH (10.0 mL) was added 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (0.094 g, 0.318 mmol). After stirred for 30 min, (4S,6S)-4-(5-amino-2,3-difluorophenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine (0.080 g, 0.244 mmol) in MeOH (10.0 mL) was added dropwise. The reaction was then stirred at room temperature for 17 h. LCMS showed about 30% remaining starting material. The reaction was quenched with saturated sodium bicarbonate solution. MeOH was removed by rotary evaporation. The aqueous residue was extracted with EtOAc (2×). The organic extracts were combined, concentrated and purified by Shimadzu HPLC to afford N-(3-((4S,6S)-2-amino-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-4-yl)-4,5-difluorophenyl)-5-cyanopicolinamide (0.041 g, 0.090 mmol, 36.7% yield) as white solid. MS m/z=458.1 [M+H]+. Calculated for C19H13F6N5O2: 457.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-440e741139574d00902d62e569014bac
Source noteuspto-grants-2016_03