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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 891050Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/891050

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
EduktTrifluoroacetic acid methylene chlorideHCID 21863450—
Edukt(2S)-1-(2-methylbenzothiazol-5-yloxy)butan-2-olHCID 69622255—
LösungsmittelAcetoneHCID 180—
LösungsmittelPotassium CarbonateHCID 11430—
Produkt(2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-olHCID 58595334—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07001909B2
Quelldatensatzuspto-grants-2006_02
ORD IDord-ae629f88f1d64d689a9a55ca7f320969
Quellennotizuspto-grants-2006_02