Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic acid, 2-chloro-, phenylmethyl ester | HCID 8786 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13913536 | HCID 13913536 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54716538 | HCID 54716538 | — |
Reaction Steps
1-(4-Hydroxybenzoyl)-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihyrocarbostyril (9 g) was suspended in DMF (90 ml). To the suspension were added potassium carbonate (2.82 g) and benzyl monochloroacetate (3.81 g) and the mixture was stirred at room temperature over night. After completion of reaction, the reaciton mixture was poured into water and extracted with dichloromethane. The extract was washed successively with water and saturated saline solution, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by silica-gel column chromatography [eluent:dichloromethane:methanol=100:0 to 100:5] to give 1-(4-benzyloxycarbonylmethoxybenzoyl)-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydroxycarbostyril (4.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04760064 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-2021021cbcd148dcad0db5eb8f57d05f |
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| Source note | uspto-grants-1988_07 |
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