Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277934Generated: October 27, 2026

Potassium bis(trimethylsilyl)amide → 2-Trifluoroacetamido-3-phenyl-6-[(E)-1-(2,3-difluorophenyl)-2-methylcarbamoylvinyl]-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/277934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant2-Trifluoroacetamido-3-phenyl-6-(2,3-difluorobenzoyl)-imidazo[1,2-a]pyridineHCID 22626759—
SolventTetrahydrofuranHCID 8028—
Product2-Trifluoroacetamido-3-phenyl-6-[(E)-1-(2,3-difluorophenyl)-2-methylcarbamoylvinyl]-imidazo[1,2-a]pyridineHCID 8675787233.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

The diethyl-(N-methylcarbamoylmethyl)phosphonate (217 mg, 1.04 mmol) in 250 mL of dry THF was placed in a flame dried flask under an argon atmosphere. The solution was cooled to −78° C. before the dropwise addition of potasium hexamethyldisilazide (5.13 mL, 2.56 mmol; 0.5 M in toluene). The mixture was stirred for 2 hours at −78° C. A solution of the 2-trifluoroacetamido-3-phenyl-6-(2,3-difluorobenzoyl)-imidazo[1,2-a]pyridine (300 mg, 0.693 mmol) in 100 mL of dry THF was added dropwise. The reaction mixture was stirred at −78° C. for 2 hours and then allowed to warm to RT. The resulting brown solution was stirred at RT for 48 hours (as it is noted a high amount of sovent was required in order to avoid dealing with heterogenous medium once the reagents were mixed). The THF was removed in vacuo and the mixture was diluted in 400 mL of EtOAc and washed with saturated NH4Cl (2×100 mL) and once with brine. After drying over MgSO4, the solvents were removed in vacuo to give a brown solid. The residue was purified by column chromatography (CH3CN:CH2Cl2, 2:1) to give 57.6 mg of product. (22%). 1H NMR, 13C NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358971B1
Source datasetuspto-grants-2002_03
ORD IDord-12cb4baedaf9452881046a4450e3c05b
Source noteuspto-grants-2002_03