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HRID 12151作成日:2026年10月24日

Toluene → 2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamide

https://huagongshe.com/ja/reaction/12151

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物2-Amino-5-chloropyridineHCID 66174—
反応物5-Chloroisatoic anhydrideHCID 78480—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
溶媒TetrahydrofuranHCID 8028—
生成物2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamideHCID 21906418100%

反応条件

温度-78 °C

反応手順

To a solution of 2-amino-5-chloropyridine (328 mg, 2.55 mmol) in tetrahydrofuran (5 ml) was 0.5M potassium bis(trimethylsilyl)amide in toluene (10 ml, 5.05 mmol) dropwise at −78° C. After stirred for additional 0.5 hr at −78° C., the mixture was added 5-chloroisatoic anhydride (0.5 g, 2.55 mmol) at −78° C. The mixture was warmed up to r.t gradually and stirred overnight. After quenched by saturated ammonium chloride solution, the mixture was extracted by ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated to give (2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide (0.71 g. 100%). MS found for C12H9Cl2N3O M+=282, (M+2)+=284.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727981B2
出典データセットuspto-grants-2010_06
ORD IDord-a9b6035cb27d4c51a725621d2aa97cec
出典メモuspto-grants-2010_06