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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 368700생성일: 2026년 10월 25일

Hydrochloric Acid → (R)-1-(2-Methoxyphenyl)-4-[2-(methyl)-2-(2-pyridinylamino)ethyl]piperazine

https://huagongshe.com/reaction/368700

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1-(2-Methoxyphenyl)piperazineHCID 1346—
반응물(R)-4-methyl-3-pyridin-2-yl[1,2,3]oxathiazolidine-2,2-dioxideHCID 22863100—
용매AcetonitrileHCID 6342—
생성물(R)-1-(2-Methoxyphenyl)-4-[2-(methyl)-2-(2-pyridinylamino)ethyl]piperazineHCID 2527306279.2%

반응 조건

온도50 °C

반응 단계

9.16 grams (46.6 millimoles) of 1-(2-methoxyphenyl)piperazine in one portion was added under argon to a solution of 10 grams (46.6 millimoles) of (R)4-methyl-3-pyridin-2-yl[1,2,3]oxathiazolidine-2,2-dioxide in 200 milliliters of acetonitrile. The mixture became yellow. After 1/2 hour, the reaction mixture was heated to 50° C. for 1 hour and then stirred at room temperature overnight. Then dilute hydrochloric acid was added. The mixture was washed with ethyl acetate, basified to pH 12 and extracted twice with ethyl acetate. The organic phases were washed with brine, dried (Mg SO4) and subjected to evaporation to give 12.053 grams of the title compound which was purified by columning in the system ethyl ether/hexane (1:1) Al2O3 to afford 9.96 grams of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06133449
출처 데이터셋uspto-grants-2000_10
ORD IDord-bf48194621b4497cb5ef0f1b6835417f
출처 메모uspto-grants-2000_10