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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39509생성일: 2026년 10월 24일

2-Fluoro-4-iodoaniline → 2-Bromo-5-[(2-fluoro-4-iodophenyl)amino]isonicotinic acid

https://huagongshe.com/ko/reaction/39509

반응식

참여 물질

역할이름HCID투입량
반응물2-Fluoro-4-iodoanilineHCID 185694—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물2-Bromo-5-fluoroisonicotinic acidHCID 46739277—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-Bromo-5-[(2-fluoro-4-iodophenyl)amino]isonicotinic acidHCID 5764964959.3%

반응 조건

온도-78 °C

반응 단계

Lithium 1,1,1,3,3,3-hexamethyldisilazan-2-ide (11.9 ml, 1.00 M, 11.82 mmol) was added to a solution of 2-fluoro-4-iodoaniline (1.40 g, 5.91 mmol) at −78° C. The pale green colored solution was stirred for 1½ h at −78° C. Then, lithium 1,1,1,3,3,3-hexamethyldisilazan-2-ide (5.45 ml, 1.00 M, 5.45 mmol) was added followed by 2-bromo-5-fluoroisonicotinic acid (1.00 g, 4.55 mmol) in THF (5 ml). The dark colored homogeneous mixture was warmed to room temperature and stirred overnight. The crude was diluted with EtOAc (300 ml). Then, it washed with dilute HCl solution (20 ml), H2O (20 ml), dried and purified on Flashmaster II using a 100 g cartridge to obtain 1.18 g (59%) of 2-Bromo-5-(2-fluoro-4-iodo-phenylamino)-isonicotinic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524911B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-e2bb8318f0b948d7804f0b05b647a69b
출처 메모uspto-grants-2013_09