Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | HCID 13236333 | HCID 13236333 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70536330 | HCID 70536330 | 119.8% |
Reaction Steps
5-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (1.96 g) and 0.20 g of sodium amide were mixed with 60 ml of DMF and stirred at room temperature for 2 hours. Then, to the mixture was added 0.67 g of allyl chloride and the mixture was stirred at room temperature for 10 hours. The reaction mixture was poured into 150 ml of saturated saline solution and organic substances were extracted with chloroform. The chloroform layer was washed with water and dehydrated. Chloroform was distilled off and the residue was purified through silica gel column chromatography followed by recrystallization from methanol-ether to give 1.76 g of 1-allyl-5-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrate, m.p. 120°-122° C., colorless granules.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04415572 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-f328352f54984c88baa18bac7314dec4 |
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| Source note | uspto-grants-1983_11 |
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