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HRID 75992作成日:2026年10月24日

Cesium carbonate → 4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamide

https://huagongshe.com/ja/reaction/75992

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-nitro-1H-pyrazoleHCID 16376—
反応物trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
反応物N-(2-bromo-5-chloro-pyridin-3-yl)-4-tert-butyl-benzenesulfonamideHCID 57942597—
触媒Copper iodideHCID 83717—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒DimethylacetamideHCID 31374—
生成物4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamideHCID 68464085—

反応手順

A solution of N-(2-bromo-5-chloro-pyridin-3-yl)-4-tert-butyl-benzene sulfonamide (534 mg, 1.32 mmol), 4-nitropyrazole (224 mg, 1.98 mmol), trans-N,N′-dimethyl-cyclohexane-1,2-diamine (42 μL, 0.264 mmol), copper iodide (51 mg, 0.264 mmol), and cesium carbonate (903 mg, 2.77 mmol) in 5 mL of N,N-dimethylacetamide was heated at 130° C. for 2 hours. Ethyl acetate and water were added and the layers were separated. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude reside was subsequently purified by flash column chromatography (0-100% ethyl acetate in hexanes) to afford 4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamide as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835468B2
出典データセットuspto-grants-2014_09
ORD IDord-f9f0f6399497473a809f2b5cef77dd9d
出典メモuspto-grants-2014_09