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HRID 218886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/218886

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US08198457B2
出典データセットuspto-grants-2012_06
ORD IDord-0c5a9bd7454d48a68e2e65f620b11977
出典メモuspto-grants-2012_06