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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | Ethanolamine | HCID 700 | — |
| 반응물 | N-(4-fluoro-3-nitrophenyl)ethanesulfonamide | HCID 3286362 | — |
| 반응물 | 1-(4,4-Difluorocyclohexyl)methanamine | HCID 15604494 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | N-(4-(((4,4-Difluorocyclohexyl)methyl)amino)-3-nitrophenyl)ethanesulfonamide | HCID 11516373 | 63.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07550495B2 |
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| 출처 데이터셋 | uspto-grants-2009_06 |
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| ORD ID | ord-98c8825b80c04d309453a53714842663 |
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| 출처 메모 | uspto-grants-2009_06 |
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