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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389150Generated: October 30, 2026

Methylamine → HCID 58243770, compound

https://huagongshe.com/reaction/389150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 58243822HCID 58243822—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 58243770HCID 58243770—

Reaction Steps

Ethyl N-[5-chloro-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy)benzoyl]glycinate (300 mg) was dissolved in ethanol (6 ml), and methylamine (2.86 ml) was added thereto, followed by stirring at room temperature for one hour. Potassium carbonate (240 mg) was added thereto, followed by stirring at 60° C. for one hour. Methylamine (2.86 ml) was added thereto, followed by stirring at 60° C. for 2 hours. The reaction solution was cooled to room temperature and water and a 1M aqueous sodium hydroxide solution were added thereto, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting solid was washed with diisopropylether to obtain, as a white solid, 5-chloro-N-[2-(methylamino)-2-oxoethyl]-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy)benzamide (131 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377923B2
Source datasetuspto-grants-2013_02
ORD IDord-3202a590fd224074aec48937e2b9d4d2
Source noteuspto-grants-2013_02