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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579754Generated: October 26, 2026

Dibenzosuberenol → 4-[4-(4-fluorophenyl)-1-piperazinyl]butyrylamino-5H-dibenzo[a,d]cycloheptene

https://huagongshe.com/reaction/579754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzosuberenolHCID 82577—
Reactant4-[4-(4-Fluorophenyl)piperazin-1-YL]butanamideHCID 20136407—
SolventAcetic AcidHCID 176—
Product4-[4-(4-fluorophenyl)-1-piperazinyl]butyrylamino-5H-dibenzo[a,d]cyclohepteneHCID 8674220457.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 200 mg of 5H-dibenzo[a,d]cyclohepten-5-ol, 300 mg of 4-[4-(4-fluorophenyl)-1-piperazinyl]butyramide and 8 ml of acetic acid is stirred at 70° C. for 20 hours. The acetic acid is distilled off under reduced pressure and 100 ml of chloroform is added to the residue. The solution is washed successively with 10% aqueous potassium carbonate solution, water and saturated aqueous sodium chloride solution, and dried over magnesium sulfate, and the chrloroform is distilled off. The residue is chromatographed on silica gel with chloroform-methanol (100:3) to give 250 mg of the title compound. m.p. 233°-235° C. (recrystallized from chloroform-n-hexane);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04749703
Source datasetuspto-grants-1988_06
ORD IDord-d8fa09e96f8d40c594cab58949f5cceb
Source noteuspto-grants-1988_06