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HRID 383781作成日:2026年10月27日

Pyrazole → 3-(1-{[2-(1H-pyrazol-1-yl)-3',5'-bis(trifluoromethyl)biphenyl-4-yl]carbonyl}pyrrolidin-3-yl)pyridine

https://huagongshe.com/reaction/383781

反応式

関与物質

役割名称HCID仕込み量
反応物PyrazoleHCID 1048—
反応物Salicylaldehyde oximeHCID 7200—
反応物Cesium carbonateHCID 10796—
反応物3-(1-{[2-Bromo-3',5'-bis(trifluoromethyl)biphenyl-4-yl]carbonyl}pyrrolidin-3-yl)pyridineHCID 86657753—
触媒HCID 178419072HCID 178419072—
溶媒AcetonitrileHCID 6342—
生成物3-(1-{[2-(1H-pyrazol-1-yl)-3',5'-bis(trifluoromethyl)biphenyl-4-yl]carbonyl}pyrrolidin-3-yl)pyridineHCID 46847591—

反応手順

A solution of 3b (54.0 mg, 0.099 mmol), pyrazole (50.7 mg, 0.745 mmol), salicylaldoxime (19.8 mg, 0.145 mmol), copper(I) oxide (16.6 mg, 0.116 mmol) and cesium carbonate (265 mg, 0.812 mmol) in acetonitrile (1.00 mL) was heated to 120° C. in a sealed microwave vial for a total of 60 min. The reaction mixture was cooled to rt, concentrated in vacuo, and the resulting crude residue was purified by preparative reversed phase HPLC on YMC Pack Pro C18 stationary phase (CH3CN/H2O as eluent, 0.05% TFA as modifier), followed by lyophilization of the purified fractions to afford the title compound 10a. m/z (ES) 531 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367679B2
出典データセットuspto-grants-2013_02
ORD IDord-a453bc123ad646129051bb5ef7295e14
出典メモuspto-grants-2013_02