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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 585064생성일: 2026년 10월 25일

Trifluoroacetic acid methylene chloride → 1-(2-Methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-ol

https://huagongshe.com/reaction/585064

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acid methylene chlorideHCID 21863450—
반응물4-[2-Hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 21935528—
용매AcetoneHCID 180—
용매Potassium CarbonateHCID 11430—
생성물1-(2-Methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-olHCID 21911691—

반응 단계

A solution of 4-[2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]-piperazine-1-carboxylic acid tert-butyl ester, a compound of formula (5) (2.0 g, 4.9 mmol), and 25% trifluoroacetic acid/methylene chloride (20 ml) was allowed to stir at room temperature overnight. The solvent was evaporated (in vacuo) to yield an oil. The oil was diluted with acetone (20 ml) and solid potassium carbonate was added until the foaming stopped. The resulting mixture was allowed to stir overnight. The solution was filtered through Celite 512, and the filtrate was evaporated (in vacuo), to yield an oil. The oil was placed under high vacuum overnight, to yield 1-(2-methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-ol, as a clear viscous oil (3.4 g. 6.3 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06930111B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-d07b9fcd9cd9436785e486ee7507f440
출처 메모uspto-grants-2005_08