HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414284Generated: November 2, 2026
Methyl Ethyl Ketone → HCID 21486936, compound
https://huagongshe.com/reaction/1414284
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | N-(2-chloroethyl)-6,7-dimethoxy-1-phenyl-3,4-dihydro-2(1H)-isoquinolinecarboxamide | HCID 21487009 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Potassium Bicarbonate | HCID 516893 | — |
| Product | HCID 21486936 | HCID 21486936 | — |
Reaction Steps
A mixture of 3.0 parts of the N-(2-chloroethyl)-6,7-dimethoxy-1-phenyl-3,4-dihydro-2(1H)-isoquinolinecarboxamide prepared in Example 8 and 4.3 parts of piperidine in approximately 40 parts of 2-butanone is heated at 65°C. for 20 hours. The reaction mixture is then stripped in vacuo and the residue taken up in dilute aqueous potassium bicarbonate solution and methylene chloride. The organic layer is dried and stripped in vacuo and the residue is crystallized from ether to afford 6,7-dimethoxy-1-phenyl-N-(2-piperidinoethyl)-3,4-dihydro-2(1H)-isoquinolinecarboxamide, melting at about 101°-102°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001244 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-d2e5ae05b0d14b81a1e414fa744f035e |
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| Source note | uspto-grants-1977_01 |
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