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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827877Generated: November 4, 2026

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

https://huagongshe.com/reaction/1827877

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ReactantHCID 69600520HCID 69600520—
SolventAcetoneHCID 180—
SolventPotassium CarbonateHCID 11430—
Product(2R)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-olHCID 29943216—

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056924B2
Source datasetuspto-grants-2006_06
ORD IDord-e176715abf4545b294689f75fd8fe195
Source noteuspto-grants-2006_06