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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1987224생성일: 2026년 10월 27일

Dimethyl Sulfoxide → N-(4-(((4,4-Difluorocyclohexyl)methyl)amino)-3-nitrophenyl)ethanesulfonamide

https://huagongshe.com/reaction/1987224

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물EthanolamineHCID 700—
반응물N-(4-fluoro-3-nitrophenyl)ethanesulfonamideHCID 3286362—
반응물1-(4,4-Difluorocyclohexyl)methanamineHCID 15604494—
용매WaterHCID 962—
생성물N-(4-(((4,4-Difluorocyclohexyl)methyl)amino)-3-nitrophenyl)ethanesulfonamideHCID 1151637363.8%

반응 조건

온도65 °C

반응 단계

N-(4-Fluoro-3-nitrophenyl)ethanesulfonamide (26 g, 0.107 mol), [(4,4-difluorocyclohexyl)methyl]amine (approx. 15 g), DIPFA (20 mL) and DMSO (100 mL) were mixed together and heated to 65° C. overnight. Ethanolamine (5 g) was added and the reaction mixture was stirred until complete disappearance of N-(4-fluoro-3-nitrophenyl)ethanesulfonamide (approx. 4-5 hrs.). The room temperature cooled down reaction mixture was poured in cold water (900 mL). The product was extracted with DCM (5×200 mL). The combined organic phases were washed with HCl 2N (3×200 mL) and dried over anhydrous Na2SO4. The solvent was removed and the crude product was purified on silica gel by flash chromatography (this material can be re-crystallized using a mixture of EtOAc and hexane) to provide the title product (24.2 g) as orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07550495B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-98c8825b80c04d309453a53714842663
출처 메모uspto-grants-2009_06