HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709261Generated: October 29, 2026
HCID 14835770, compound → HCID 14835771, compound
https://huagongshe.com/reaction/1709261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 14835770 | HCID 14835770 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14835771 | HCID 14835771 | — |
Reaction Steps
7.0 g of 3-nitro-5-[4-{(E)-3-(3-triphenylmethylaminophenyl)allyl}piperazin-1-yl]-10,11-dihydro-5H-dibenzo[a,d]cycloheptene was dissolved in 20 ml of acetic acid and 20 ml of methanol. The solution was stirred for 2 hours at 40° C. The solvent was removed by distillation under reduced pressure. The residue was dissolved in 100 ml of ethyl acetate. The solution was washed with a saturated aqueous sodium hydrogen-carbonate solution, water and a saturated aqueous sodium chloride solution in this order and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by a column chromatography (eluant: chloroform/ethanol=50/1) to obtain 3.77 g of light yellow solid 3-nitro-5-[4-{(E)-3-(3-aminophenyl)allyl}-piperazin-1-yl]-10,11-dihydro-5H-dibenzo[a,d]cycloheptene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04948796 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-6dab5968fcea45678e5f428292347f5d |
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| Source note | uspto-grants-1990_08 |
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