Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 2-Oxindole-5-carboxylic acid | HCID 2773318 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13649190 | HCID 13649190 | 57.4% |
Reaction Steps
5-Carboxyoxindol (0.93 g) and 0.8 ml of trimethylamine were suspended in 10 ml of tetrahydrofuran (THF), and a solution of 1.0 g of diethylchlorophosphate in 10 ml of THF was added dropwise thereto at room temperature with stirring. The mixture was stirred for 3 hours at room temperature. To the mixture was added dropwise a solution of 1.1 g of benzylpiperazine in 10 ml of THF and was further stirred for 10 hours at room temperature. After completion of reaction, crystals which precipitated were filtered off and the filtrate was concentrated. To the residue was added a saturated aqueous solution of sodium hydrogencarbonate and the mixture was extracted with chloroform. Organic layer was washed with water and a saturated saline solution, dried over anhydrous sodium sulfate, and the solvent was distilled off. Recrystallization of the residue from isopropyl alcohol gave 1.01 g of 5-(4-benzyl-1-piperazinylcarbonyl)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-1f42e14d392f4ad1bbe108c5e3bb8488 |
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| Source note | uspto-grants-1988_04 |
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