HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703447Generated: October 31, 2026
Sodium Hydroxide → HCID 14624991, compound
https://huagongshe.com/reaction/703447
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(7-Methoxynaphthalen-1-yl)piperazine | HCID 14566720 | — |
| Reactant | HCID 14624973 | HCID 14624973 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14624991 | HCID 14624991 | 87.5% |
Reaction Steps
1.5 g (7.15 mmol) of (±)-4-(2-chloroethyl)-3,4-dihydro-2(1H)-quinolinone are mixed intimately with 3.65 g (15 mmol) of 1-(7-methoxy-1-naphthyl)piperazine and the mixture is heated to 130° C. for 1 h while stirring. The cooled residue is taken up between 25 ml of 2N sodium hydroxide and twice 50 ml of dichloromethane. The organic extract is washed with water, dried over magnesium sulphate and concentrated. The residue is purified by elution with a dichloromethane/methanol (95:5) mixture on a silica column. The purified fraction is crystallized in ether and this solid is drained and dried. 2.6 g (87.5%) of (±)-4-{2-[4-(7-methoxy-1-naphthyl)-1-piperazinyl]ethyl}-3,4-dihydro-2(1H)-quinolinone, melting point 177°-178° C., are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983607 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-99a2bcedfc4a4c248e5482ec2af3d8e0 |
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| Source note | uspto-grants-1991_01 |
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