HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484312Generated: October 31, 2026
Potassium Hydroxide → HCID 19747323, compound
https://huagongshe.com/reaction/484312
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 11-(1-Methylpiperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine-8-carbonitrile | HCID 3072648 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19747323 | HCID 19747323 | 66% |
Reaction Steps
Ethanol (150 ml) was added to 2 g of 8-cyano-11-(1-methyl-4-piperidylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine so that the latter was dissolved in the former. An aqueous solution of 2.8 g of potassium hydroxide was added further, followed by reflux for 3.5 hours. After the reaction, the solvent was distilled off under reduced pressure and a brine was added to the residue, followed by extraction with chloroform. The extract was dried over anhydrous Na2SO4 and then filtered. The filtrate was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column and, from relevant fractions eluted with chloroform:methanol 25:1 and 10:1), 1.4 g of 11-(1-methyl-4-piperidylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine-8-carboxamide were obtained (yield: 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05231101 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-b42b2f3b98584253b8da0faf4292356c |
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| Source note | uspto-grants-1993_07 |
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