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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43372생성일: 2026년 10월 23일

Hydrochloric Acid → (3R)-3-Methyl-1-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine

https://huagongshe.com/ko/reaction/43372

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,4-DioxaneHCID 31275—
반응물DiisopropylethylamineHCID 81531—
반응물4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
반응물tert-Butyl (2R)-2-methylpiperazine-1-carboxylateHCID 10262201—
용매DichloromethaneHCID 6344—
생성물(3R)-3-Methyl-1-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazineHCID 5915211482.8%

반응 단계

To a solution of 1,1-dimethylethyl (2R)-2-methyl-1-piperazinecarboxylate (2.95 g, 14.73 mmol) in DCM (120 ml) was added DIPEA (5.40 ml, 30.9 mmol) and then 4-(trifluoromethyl)benzenesulfonyl chloride (3.96 g, 16.20 mmol). The reaction mixture was stirred 2.5 hours at room temperature then washed with water (250 ml), dried on a phase separation cartridge and concentrated in vacuo. The obtained product was dissolved in 1,4-dioxane (60 ml) and treated with 4M aq. HCl in 1,4-dioxane (18.41 ml, 73.6 mmol) overnight. The mixture was concentrated under vacuo then dissolved in EtOAc (150 ml), washed with 2N aq. NaOH solution (200 ml) then dried on a phase separation cartridge and concentrated in vacuo. The product was then dissolved in EtOAc (100 ml) and extracted with 2M aq. HCl (2×200 ml). 2M aq. NaOH solution was added to the aqueous layer until basic pH then the product was extracted with EtOAc (500 ml). The organic layer was dried on a phase separation cartridge and concentrated under vacuo to give the title compound (3.76 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536183B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a35744ef925e4e3d906abb73e0363e80
출처 메모uspto-grants-2013_09