돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2080471생성일: 2026년 10월 27일

Acetonitrile → [5-Chloro-4-[(4-chlorophenylsulfonyl)(2,5-difluorophenyl)methyl]pyridin-2-yl]amine

https://huagongshe.com/reaction/2080471

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Ceric ammonium nitrateHCID 180504—
반응물Sodium BicarbonateHCID 516892—
반응물5-Chloro-4-[(4-chlorophenylsulfonyl)(2,5-difluorophenyl)methyl]-2-(3,4-dimethoxybenzylamino)pyridineHCID 23114751—
용매WaterHCID 962—
생성물[5-Chloro-4-[(4-chlorophenylsulfonyl)(2,5-difluorophenyl)methyl]pyridin-2-yl]amineHCID 2311467138%

반응 단계

To an acetonitrile (4 ml)/water (1 ml) mixed solution of the 5-chloro-4-[(4-chlorophenylsulfonyl)(2,5-difluorophenyl)methyl]-2-(3,4-dimethoxybenzylamino)pyridine (43 mg, 0.074 mmol) obtained in Example 186 was added cerium (IV) diammonium nitrate (100 mg) under ice cooling. The resulting mixture was stirred for 1.5 hours. To the reaction mixture was added saturated sodium bicarbonate, followed by extraction with methylene chloride. The organic layer was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure. The residue thus obtained was purified by silica gel thin-layer chromatography (hexane:ethyl acetate=3:1) to give the title compound (12 mg, 0.028 mmol, 38%) as a pale yellowish white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07932271B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-2ff93e0a106c4ac5bac60f62f77092a8
출처 메모uspto-grants-2011_04