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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218459생성일: 2026년 10월 24일

Iodine → 5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide

https://huagongshe.com/ko/reaction/218459

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물BistrifluoroacetoxyiodobenzeneHCID 12041285—
반응물N-Methoxy-N-methyl-1H-indazole-3-carboxamideHCID 16036867—
반응물Sodium BisulfiteHCID 23665763—
용매DichloromethaneHCID 6344—
생성물5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamideHCID 2058073872%

반응 단계

To a solution of N-methoxy-N-methyl-1H-indazole-3-carboxamide (12.4 g, 60.42 mmol) in CH2Cl2 (200 mL) was added bis(trifluoroacetoxy)iodobenzene (28.78 g, 66.74 mmol), followed by dropwise addition of iodine (9.22 g, 36.33 mmol) in CH2Cl2 at rt. The reaction was stirred overnight, after which 300 mL saturated NaHSO3 was added and a solid began to precipitate, which was then filtered. The filtrate was concentrated and triturated with a small amount of CH2Cl2. The combined solids were dried to give 5-iodo-N-methoxy-N-methyl-1H-indazole-3-carboxamide (14.4 g, 72%) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198456B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-bf0c526919e04f2bb8dbe14fc2f2e7db
출처 메모uspto-grants-2012_06