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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606800Generated: October 27, 2026

Potassium Sodium Tartrate → 5-(3-Fluorophenylethynyl)-N-methoxy-N-methylnicotinamide

https://huagongshe.com/reaction/606800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Sodium TartrateHCID 9357—
ReactantN,O-DimethylhydroxylamineHCID 14232—
ReactantTrimethylaluminumHCID 16682925—
Reactant5-(3-Fluorophenylethynyl)-nicotinic acid ethyl esterHCID 67047762—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product5-(3-Fluorophenylethynyl)-N-methoxy-N-methylnicotinamideHCID 8662246733.2%

Reaction Steps

Sequentially add a 2 M solution of trimethylaluminum in toluene (0.64 g, 8.91 mmol) and 5-(3-fluorophenylethynyl)-nicotinic acid ethyl ester (0.24 g, 0.89 mmol), (prepared essentially as described in PREPARATION 17), to a solution of N,O-dimethylhydroxylamine (0.435 g, 4.46 mmol) in anhydrous toluene (4.0 mL) at 0° C. After 30 min, warm to room temperature and stir overnight. Dilute the reaction with ethyl acetate and an aqueous saturated solution of Rochelle salt (potassium sodium tartrate) and stir vigorously for 1 h. Separate the organic layer; dry (magnesium sulfate), filter and concentrate. Purify the resulting residue by silica gel chromatography, eluting with a linear gradient of 100:0 to 60:40 tetrahydrofuran:hexanes, to give the title compound as a pale yellow oil (0.084 g, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915424B2
Source datasetuspto-grants-2011_03
ORD IDord-587fed56830847d1b4748c7a75299f09
Source noteuspto-grants-2011_03