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HRID 522126作成日:2026年10月25日

Pyridine → 5-(5-bromo-2-chlorobenzamido)-N-cyclopropyl-1-phenyl-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/522126

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Potassium CarbonateHCID 11430—
反応物CyclopropylamineHCID 69828—
反応物Propylphosphonic acidHCID 204484—
反応物5-(5-bromo-2-chlorobenzamido)-1-phenyl-1H-pyrazole-3-carboxylic acidHCID 118456238—
溶媒HCID 178479889HCID 178479889—
生成物5-(5-bromo-2-chlorobenzamido)-N-cyclopropyl-1-phenyl-1H-pyrazole-3-carboxamideHCID 118456026131.4%

反応手順

To 5-(5-bromo-2-chlorobenzamido)-1-phenyl-1H-pyrazole-3-carboxylic acid (Preparation 12, 200 mg, 0.48 mmol), cyclopropylamine (137 mg, 2.40 mmol) and pyridine (114 mg, 1.44 mmol) in methyl THF (5 mL) was added 1-propylphosphonic acid cyclic anhydride (50% solution in EtOAc, 0.48 mL, 0.82 mmol) at room temperature. The reaction was stirred at room temperature for 17 hours. A 2M aqueous solution of potassium carbonate was added until the pH became basic and the solution was extracted with EtOAc (3×15 mL). The combined organic layers were concentrated in vacuo and the residue was purified by silica gel column chromatography eluting with EtOAc to afford the title compound (290 mg, 88%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328096B2
出典データセットuspto-grants-2016_05
ORD IDord-05189135f75246cd9c30df9d9100c3b1
出典メモuspto-grants-2016_05