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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibenzosuberenol | HCID 82577 | — |
| Reactant | 4-[4-(4-Fluorophenyl)piperazin-1-YL]butanamide | HCID 20136407 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-[4-(4-fluorophenyl)-1-piperazinyl]butyrylamino-5H-dibenzo[a,d]cycloheptene | HCID 86742204 | 57.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04749703 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-d8fa09e96f8d40c594cab58949f5cceb |
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| Source note | uspto-grants-1988_06 |
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