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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1873839생성일: 2026년 10월 25일

Diisopropylethylamine → 1-[2-(Methylsulfonyl)-4-(trifluoromethoxy)benzoyl]-4-(1-methyl-1-{[3-(trifluoromethyl)phenyl]sulfonyl}ethyl)piperidine

https://huagongshe.com/reaction/1873839

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물HCID 59447309HCID 59447309—
반응물4-(1-Methyl-1-{[3-(trifluoromethyl)phenyl]sulfonyl}ethyl)piperidineHCID 59447409—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Trifluoroacetic acidHCID 6422—
생성물1-[2-(Methylsulfonyl)-4-(trifluoromethoxy)benzoyl]-4-(1-methyl-1-{[3-(trifluoromethyl)phenyl]sulfonyl}ethyl)piperidineHCID 25255784—

반응 단계

To a 10 ml vial was added 4-(1-methyl-1-{[3-(trifluoromethyl)phenyl]sulfonyl}ethyl)piperidine (70.8 mg, 0.211 mmol), 2-(methylsulfonyl)-4-(trifluoromethoxy)benzoic acid (50 mg, 0.176 mmol), Bop reagent (93 mg, 0.211 mmol), diisopropylethyl amine (0.062 ml, 0.352 mmol) and 2 ml dimethylformamide. The resulting solution was stirred at room temperature for 10 minutes. The reaction mixture was diluted with 1 ml dimethyl sulfoxide, 1 ml water and 0.03 ml of trifluoroacetic acid. This mixture was loaded on a reverse phase column and purified with HPLC eluted with water/acetonitrile gradient solvent. Desired fraction was collected and lyophilized to give to give title compound as fluffy white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304434B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-66f474659cc04294a5f14145823fbc0c
출처 메모uspto-grants-2012_11