HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648973Generated: October 26, 2026
Water → 5-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]oxindol
https://huagongshe.com/reaction/648973
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Veratroyl chloride | HCID 77070 | — |
| Reactant | 5-(1-Piperazinyl)oxindol.hydrobromide | HCID 13646031 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]oxindol | HCID 13646032 | 58.6% |
Reaction Steps
5-(1-Piperazinyl)oxindol.hydrobromide (2.0 g) was suspended in 30 ml of N,N-dimethylformamide (DMF), and 2.3 ml of triethylamine was added thereto subsequently. The mixture was cooled to 0° to 5° C. To the mixture was added dropwise 5 ml of DMF solution containing 1.5 g of 3,4-dimethoxybenzoyl chloride at the same temperature as above with stirring. After completion of addition, the mixture was stirred at room temperature for one hour. The reaction mixture was poured into a large amount of water and extracted with chloroform. After washing with water, the extract was dried over anhydrous sodium sulfate and chloroform was removed by distillation. The residue was purified by silica-gel column chromatography (eluent: chloroform:methanol=100:1) and recrystallized from methanol to give 1.5 g of 5-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]oxindol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04737501 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-dfe06f226bbe4c7c89f875369a1139db |
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| Source note | uspto-grants-1988_04 |
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