돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 891050생성일: 2026년 10월 25일

tert-Butyl piperazine-1-carboxylate → (2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-ol

https://huagongshe.com/reaction/891050

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물Trifluoroacetic acid methylene chlorideHCID 21863450—
반응물(2S)-1-(2-methylbenzothiazol-5-yloxy)butan-2-olHCID 69622255—
용매AcetoneHCID 180—
용매Potassium CarbonateHCID 11430—
생성물(2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-olHCID 58595334—

반응 단계

A solution of (2S)-1-(2-methylbenzothiazol-5-yloxy)butan-2-ol, tert butyl piperazinecarboxylate, 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 (2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-ol, as a clear viscous oil (3.4 g. 6.3 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07001909B2
출처 데이터셋uspto-grants-2006_02
ORD IDord-ae629f88f1d64d689a9a55ca7f320969
출처 메모uspto-grants-2006_02