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HRID 78779생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/78779

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-4-iodoanilineHCID 282930—
반응물3-Fluoropyridine-4-carboxylic acidHCID 345361—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매TetrahydrofuranHCID 8028—
생성물3-[(2-Chloro-4-iodophenyl)amino]isonicotinic acidHCID 57649651—

반응 단계

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%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841459B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-23b0b8c07ba843b6af0aaf18ece7b1a3
출처 메모uspto-grants-2014_09