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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417954Generated: October 29, 2026

Piperazine → HCID 15409320, compound

https://huagongshe.com/reaction/1417954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
ReactantNaphth[1,2-c]isoxazole, 3-chloro-4,5-dihydro-HCID 10987412—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 15409320HCID 15409320—

Reaction Steps

A stirred mixture of 3-chloro-4,5-dihydronaphth[1,2-c]isoxazole (5.0 g, 24.4 mmol), piperazine(34.2 g, 397.7 mmol) and K2CO3 (6.73 g, 48.7 mmol) in 40 ml of N-methylpyrrolidinone under N2 was lowered into an oil bath preheated to 150° C. The mixture was heated while stirring under N2 for 45 minutes. At that time, TLC (CH2Cl2) showed no remaining starting material. The mixture was removed from the heating bath, allowed to cool to room temperature and extracted with Et2O. This organic phase was washed twice with H2O, dried over MgSO4, filtered and concentrated in vacuo to obtain a crude solid. The solid was collected, recrystallized from heptane/Et2O and dried in vacuo (0.1 mm) at 85° C. to provide pure product, mp of 97°-99° C., homogeneous by TLC [silica, 1:1 CH3OH:CH2Cl2, Rf=0.35]. The IR (CHCl3), NMR (CDCl3) and Mass Spectrum (M+ =255, EI, 70 ev) were consistent with the structure. The yield was 3.372 g (13.22 mmol, 54.19%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05880121
Source datasetuspto-grants-1999_03
ORD IDord-49e3cbb6d7104d18886c202e8f79819b
Source noteuspto-grants-1999_03