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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627483Generated: October 29, 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → N-methoxy-N-methyl-6-(trifluoromethyl)nicotinamide

https://huagongshe.com/reaction/627483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-(Trifluoromethyl)nicotinoyl chlorideHCID 2777557—
SolventDichloromethaneHCID 6344—
ProductN-methoxy-N-methyl-6-(trifluoromethyl)nicotinamideHCID 23116945—

Reaction Conditions

Temperature7 °C

Reaction Steps

To a 1 L 3-neck flask equipped with an overhead stirrer, Claisen adaptor, nitrogen bubbler, 125 mL addition funnel, and thermocouple was added 6-(trifluoromethyl)nicotinoyl chloride (49.3 g, 235.2 mmol, Intermediate 15, step a), dichloromethane (493 mL), and N,O-dimethylhydroxylamine hydrochloride (25.63 g, 258.8 mmol). After the mixture was cooled to 7° C., diisopropylethylamine (90.263 mL, 517.6 mmol) was added such that the addition temperature did not exceed 16° C. After the addition, the reaction was allowed to warm to room temperature. The reaction was then transferred to a separatory funnel and the organic layer was washed with saturated NaHCO3 (2×100 mL) followed by water (100 mL) and then dried over sodium sulfate, and filtered. Solvent removal afforded the title compound as a brownish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309222B2
Source datasetuspto-grants-2016_04
ORD IDord-fde3b950c42d496e90e406e6542c9d1c
Source noteuspto-grants-2016_04