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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41307생성일: 2026년 10월 24일

Water → 1-[(3-Methyl-2-pyridinyl)carbonyl]-4-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine

https://huagongshe.com/ko/reaction/41307

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물3-Methylpicolinic acidHCID 268757—
반응물1-[4-(Trifluoromethyl)benzenesulfonyl]piperazineHCID 2554578—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물1-[(3-Methyl-2-pyridinyl)carbonyl]-4-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazineHCID 4461196164.7%

반응 단계

To a solution of 1-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine (Description 1) (100 mg, 0.340 mmol) in DMF (5 ml) was added HOBT.H2O (52.0 mg, 0.340 mmol), HBTU (129 mg, 0.340 mmol), 3-methyl-2-pyridinecarboxylic acid (46.6 mg, 0.340 mmol) and DIPEA (0.178 ml, 1.019 mmol). The reaction mixture was stirred for 2 hours at room temperature. Reaction mixture was transferred to a 100 ml round bottom flask and was reduced to dryness in vacuo. The residue was dissolved in DCM (50 ml) and transferred to a separating funnel then was washed with saturated aq. NaHCO3 solution (5 ml), twice. The organic layer was collected and dried with dried magnesium sulphate. The solid was removed by filtration and the filtrate collected in a 250 ml round bottom flask and reduced to dryness in vacuo. The residue was then dissolved in 1.8 ml 1:1 MeCN/DMSO and purified by MDAP in 2 batches. The fractions containing desired product were combined in a 250 ml round bottom flask and reduced in vacuo to yield the title compound (91 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530478B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a0dae1b96ba14871af6017fb09c888d8
출처 메모uspto-grants-2013_09