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HRID 39518作成日:2026年10月27日

2-Chloro-4-iodoaniline → 3-[(2-Chloro-4-iodophenyl)amino]isonicotinic acid

https://huagongshe.com/reaction/39518

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-4-iodoanilineHCID 282930—
反応物3-Fluoropyridine-4-carboxylic acidHCID 345361—
反応物Lithium HexamethyldisilazideHCID 2733832—
溶媒TetrahydrofuranHCID 8028—
生成物3-[(2-Chloro-4-iodophenyl)amino]isonicotinic acidHCID 57649651—

反応手順

To suspension of 3-fluoroisonicotinic acid (2.00 g, 14.17 mmol, in tetrahydrofuran (50 ml) at −78° C. was added lithium bis(trimethylsilyl)amide (14.3 ml, 17.01 mmol). The dark colored suspension was stirred for 15 min. In another flask, to a solution of 2-chloro-4-iodoaniline (4.7 g, 18.43 mmol) in THF (50 ml) was added lithium bis(trimethylsilyl)amide (24.9 ml, 29.77 mmol) at −78° C. under N2. The resulting green colored solution was stirred for 15 min. To this green colored solution the lithiated acid solution was added. The cold bath was removed, allowed to warm to room temperature, and stirred overnight. The mixture was filtered, and the crude was diluted with EtOAc (400 ml). It was then washed with dilute HCl (25 ml), H2O (25 ml), and dried. During concentration of the solvent, 3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid was separated out as an yellow solid. (1.3 g, 24%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524911B2
出典データセットuspto-grants-2013_09
ORD IDord-67a1f29fed714bb4aa9e2cab3928e5b7
出典メモuspto-grants-2013_09