Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459425Generated: November 1, 2026

Tert-butyl 4-(4-(4-(1,1-dimethylethoxycarbonyl)piperazin-1-yl)phenylaminocarbonyl)phenoxyacetate → 4-(4-(Piperazin-1-yl)phenylaminocarbonyl)phenoxyacetic acid

https://huagongshe.com/reaction/1459425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(4-(4-(1,1-dimethylethoxycarbonyl)piperazin-1-yl)phenylaminocarbonyl)phenoxyacetateHCID 53850602—
SolventEthyl AcetateHCID 8857—
Product4-(4-(Piperazin-1-yl)phenylaminocarbonyl)phenoxyacetic acidHCID 5408293640.4%

Reaction Steps

To a 100 mL round bottomed flask with a stirring bar and a gas dispersion tube was added tert-butyl 4-(4-(4-(1,1-dimethylethoxycarbonyl)piperazin-1-yl)phenylaminocarbonyl)phenoxyacetate (0.78 g, 1.52 mmol) and EtOAc (40 mL). This solution was cooled in an ice bath and HCl gas was sparged through the solution for 15 min. The resulting mixture was aged 90 min. The excess HCl and EtOAc were removed in vacuo and the crude product was purified by preparative reverse phase HPLC. There was obtained 0.218 g of 4-(4-(piperazin-1-yl)phenylaminocarbonyl)phenoxyacetic acid as a crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854245
Source datasetuspto-grants-1998_12
ORD IDord-0c649915052b432592e80879a007e83e
Source noteuspto-grants-1998_12