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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352323Generated: October 30, 2026

3,5-Bis(trifluoromethyl)benzyl bromide → N-(3,5-Bis-trifluoromethyl-benzyl)-N-methyl-6-morpholin-4-yl-4-o-tolyl-nicotinamide

https://huagongshe.com/reaction/352323

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantN-methyl-6-morpholin-4-yl-4-o-tolyl-nicotinamideHCID 22479279—
SolventTetrahydrofuranHCID 8028—
ProductN-(3,5-Bis-trifluoromethyl-benzyl)-N-methyl-6-morpholin-4-yl-4-o-tolyl-nicotinamideHCID 1011954444%

Reaction Steps

To a solution of 0.27 g (0.87 mmol) N-methyl-6-morpholin-4-yl-4-o-tolyl-nicotinamide in 15 ml tetrahydrofuran, 1.12 ml of a 1 M solution (1.12 mmol) of potassium hexamethyldisilazide in tetrahydrofuran was added at 0° C. After 30 min, 0.16 ml (0.87 mmol) 3,5-bis(trifluoromethyl)benzyl bromide were added dropwise and the reaction mixture was allowed to warm to room temperature over night. Quenching with water was followed by extraction with ethyl acetate. The combined organic extracts were dried with sodium sulfate and concentrated. Column chromatography gave 0.20 g (44%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747026B2
Source datasetuspto-grants-2004_06
ORD IDord-3e90fb89f8df4bdaa69a9e59c96a3969
Source noteuspto-grants-2004_06