돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271224생성일: 2026년 10월 27일

4-[2-Hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]-piperazine-1-carboxylic acid tert-butyl ester → (2R)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-ol

https://huagongshe.com/reaction/271224

반응식

참여 물질

역할이름HCID투입량
반응물4-[2-Hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 21935528—
용매Hydrochloric AcidHCID 313—
용매1,4-DioxaneHCID 31275—
생성물(2R)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-olHCID 29943216—

반응 단계

A solution of 4-[2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]-piperazine-1-carboxylic acid tert-butyl ester (2.9 g, 7.1 mmol), a compound of formula (5), was dissolved in a 4N solution of HCl in dioxane (20 ml) and allowed to stir at room temperature for 4 hours. The solvent was evaporated under reduced pressure to yield a white solid. The white solid was dried under high vacuum, and then dissolved in methanol (250 ml). AG 1-X8 resin was added and the mixture shaken. Additional resin was added until a neutral pH was obtained. The resin beads were removed by filtration, and methanol removed from the filtrate under reduced pressure, and the residue placed under high vacuum overnight, to yield (2R)-3-(2-methylbenzothiazol-5-yloxy)-1-piperazinylpropan-2-ol as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452889B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-da0dde98791a4e7bbda0176abbb27583
출처 메모uspto-grants-2008_11