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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051008Generated: October 31, 2026

Piperazine → 7-Methyl-3-(1-piperazinyl)-1,2-benzisoxazole

https://huagongshe.com/reaction/2051008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant3-Chloro-7-methylbenzo[d]isoxazoleHCID 15057448—
Solvent1-ButanolHCID 263—
Product7-Methyl-3-(1-piperazinyl)-1,2-benzisoxazoleHCID 1505744971.5%

Reaction Steps

To a stirred and heated (90° C.) mixture of 120 parts of piperazine and 400 parts of 1-butanol were added dropwise 60 parts of 3-chloro-7-methyl-1,2-benzisoxazole. Upon complete addition, stirring was continued for 6 hours at reflux temperature. After cooling, the reaction mixture was filtered and the filtrate was evaporated. The residue was taken up in water and the product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was solidified on standing, yielding 56 parts (71.5%) of 7-methyl-3-(1-piperazinyl)-1,2-benzisoxazole as a residue (int. 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015740
Source datasetuspto-grants-1991_05
ORD IDord-3ff57a959cfe47f1a43a7fd019b5bdb5
Source noteuspto-grants-1991_05