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HRID 876327作成日:2026年10月26日

Potassium Carbonate → N-(1-{[(2R,5R)-2,5-Dimethylpyrrolidin-1-yl]carbonyl}-5-[4-(trifluoromethyl)phenyl]piperidin-3-yl)benzenecarboxamide

https://huagongshe.com/reaction/876327

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2,5-Dimethylpyrrolidine, (2R,5R)-HCID 641767—
反応物4-Nitrophenyl 3-[(phenylcarbonyl)amino]-5-[4-(trifluoromethyl)phenyl]piperidine-1-carboxylateHCID 66701467—
溶媒DimethylformamideHCID 6228—
生成物N-(1-{[(2R,5R)-2,5-Dimethylpyrrolidin-1-yl]carbonyl}-5-[4-(trifluoromethyl)phenyl]piperidin-3-yl)benzenecarboxamideHCID 66701509—

反応手順

80 mg (0.16 mmol) of 4-nitrophenyl 3-[(phenylcarbonyl)amino]-5-[4-(trifluoromethyl)phenyl]piperidine-1-carboxylate were initially charged in 1.7 ml of DMF, and 46 mg (0.47 mmol) of (2R,5R)-2,5-dimethylpyrrolidine and 22 mg (0.16 mmol) of potassium carbonate were added. The mixture was reacted in a microwave (Emrys Optimizer) at 150° C. for 15 min. The crude product was then purified by preparative HPLC (Reprosil C18, water/acetonitrile gradient). Yield: 12 mg (15% of theory)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08987248B2
出典データセットuspto-grants-2015_03
ORD IDord-e885d12d431148998792d011cdba7707
出典メモuspto-grants-2015_03