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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835335Generated: October 31, 2026

Potassium bis(trimethylsilyl)amide → 2-[3,5-bis(trifluoromethyl)phenyl]-N-[6-chloro-4-(2-chlorophenyl)-3-pyridinyl]-N,2-dimethylpropanamide

https://huagongshe.com/reaction/1835335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant2-(3,5-Bis(trifluoromethyl)phenyl)-2-methylpropanoyl chlorideHCID 11267141—
Reactant[6-Chloro-4-(2-chloro-phenyl)-pyridin-3-yl]-methyl-amineHCID 23502811—
SolventTetrahydrofuranHCID 8028—
Product2-[3,5-bis(trifluoromethyl)phenyl]-N-[6-chloro-4-(2-chlorophenyl)-3-pyridinyl]-N,2-dimethylpropanamideHCID 2350283767%

Reaction Steps

To a solution of 180 mg (0.711 mmol) [6-chloro-4-(2-chloro-phenyl)-pyridin-3-yl]-methyl-amine in 7 ml dry tetrahydrofuran 0.86 ml of a 0.91 M solution (0.78 mmol) of potassium hexamethyldisilazide in tetrahydrofuran was added at room temperature under an atmosphere of argon. After 45 min 295 mg (0.924 mmol) 2-(3,5-bis-trifluoromethyl-phenyl)-2-methyl-propionyl chloride were added. The reaction mixture was stirred at room temperature for 3 h. Quenching with water was followed by dilution with tert-butyl methyl ether and washing with 2 M aqueous sodium carbonate solution and brine. The combined aqueous layers were extracted with two portions of tert-butyl methyl ether. The combined organic extracts were dried with sodium sulfate and concentrated. Flash chromatography gave 254 mg (67%) of the title compound as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770637B2
Source datasetuspto-grants-2004_08
ORD IDord-3e4ded52720c4178872967328eb7935c
Source noteuspto-grants-2004_08