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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271227Generated: October 27, 2026

4-Chlorobutyl phenyl ether → (2R)-3-(2-methylbenzothiazol-5-yloxy)-1-[4-(4-phenoxybutyl)piperazinyl]propan-2-ol

https://huagongshe.com/reaction/271227

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobutyl phenyl etherHCID 75857—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(2-Methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-olHCID 21911691—
SolventEthanolHCID 702—
Product(2R)-3-(2-methylbenzothiazol-5-yloxy)-1-[4-(4-phenoxybutyl)piperazinyl]propan-2-olHCID 11236403—

Reaction Conditions

Temperature88 °C

Reaction Steps

(4-Chlorobutoxy) benzene (320 mg, 1.39 mmol) in EtOH (17 Ml) was treated with DIEA (0.48 Ml, 2.78 mmol) and 1-(2-methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-ol as prepared in Example 3A (427 mg, 1.39 mmol), then stirred 14 hours at 88° C. Upon cooling, concentrated in vacuo and purified on the Isco™ (10 g Redisep™ columns, 100% EtOAc hold 2 min., 8 min. gradient to 20% MeOH/EtOAc, hold 10 min) to provide (2R)-3-(2-methylbenzothiazol-5-yloxy)-1-[4-(4-phenoxybutyl)piperazinyl]propan-2-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452889B2
Source datasetuspto-grants-2008_11
ORD IDord-a29355d194d443fc95e9e5ce6571b6a8
Source noteuspto-grants-2008_11