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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 453326생성일: 2026년 10월 25일

Trifluoromethylsulfonamide → N-(3-{1-[5-Chloro-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazol-3-YL}-propionyl)-C,C,C-trifluoro-methanesulfonamide

https://huagongshe.com/reaction/453326

반응식

참여 물질

역할이름HCID투입량
반응물TrifluoromethylsulfonamideHCID 79001—
반응물3-{1-[5-Chloro-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazol-3-YL}-propionyl fluorideHCID 86667289—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물N-(3-{1-[5-Chloro-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazol-3-YL}-propionyl)-C,C,C-trifluoro-methanesulfonamideHCID 8666728872%

반응 단계

To a solution of acid fluoride 9 (0.14 g, 0.33 mmol) and DMAP 0.161 g (1.3 mmol) in dry DCM, trifluoromethanesulfonamide 0.147 g (0.98 mmol) was added. The mixture was stirred under a nitrogen atmosphere for 16 hours before diluting with EtOAc. The organic phase was washed with 2M HCl, followed by brine, dried over MgSO4 and evaporated to dryness. The crude acyl sulphonamide 10 was purified on silica to yield 0.13 g as a white solid (72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492424B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-e0210d42a02c48f8befebabf8b50faf8
출처 메모uspto-grants-2013_07