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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227007Generated: October 26, 2026

Water → 2,2,2-Trifluoro-N-{6-[3-(4-methoxy-3-methyl-benzoyl)-4-oxo-4H-quinolin-1-ylmethyl]-pyridin-2-yl}-acetamide

https://huagongshe.com/reaction/227007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSilanamine, 1,1,1-trimethyl-N-(trimethylsilyl)-, potassium saltHCID 45051783—
ReactantN-(6-bromomethyl-pyridin-2-yl)-2,2,2-trifluoro-acetamideHCID 57754672—
Reactant3-(4-Methoxy-3-methyl-benzoyl)-1H-quinolin-4-oneHCID 57754758—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2,2,2-Trifluoro-N-{6-[3-(4-methoxy-3-methyl-benzoyl)-4-oxo-4H-quinolin-1-ylmethyl]-pyridin-2-yl}-acetamideHCID 57754779173.9%

Reaction Steps

Potassium hexamethyldisilazane (2.44 mL, 1.22 mmol, 0.5 M in THF) was added to a solution of 3-(4-Methoxy-3-methyl-benzoyl)-1H-quinolin-4-one (0.30 g, 1.02) in 10 mL of tetrahydrofuran. After the reaction was stirred at rt for 20 minutes, N-(6-Bromomethyl-pyridin-2-yl)-2,2,2-trifluoro-acetamide (0.35 g, 0.246 mmol) was added and stirred overnight at room temperature. Water and ethyl acetate were added and the two phases were separated. The aqueous phase was extracted with ethyl acetate (3×20 mL). The combined organic layers were dried with magnesium sulfate, filtered and concentrated in vacuo. The crude brown solid was purified by reverse phase HPLC with a C18 column, gradient of 20-70% acetonitrile—0.1% TFA to yield 212 mg of 2,2,2-Trifluoro-N-{6-[3-(4-methoxy-3-methyl-benzoyl)-4-oxo-4H-quinolin-1-ylmethyl]-pyridin-2-yl}-acetamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-5f6f8193a68d4a29bb42c0a7c9495ae6
Source noteuspto-grants-2009_07