Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isatin | HCID 7054 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 23363873 | HCID 23363873 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23363840 | HCID 23363840 | — |
Reaction Steps
1H-Indole-2,3-dione (2.9 g) in dry DMF (5 ml) at 0° C. was treated with sodium hydride (80% dispersion in mineral oil, 600 mg). The mixture was warmed to 40° C. and after 45 minutes a solution of 1-(2-chloroethyl)-4-[(4-fluorophenyl)methyl]piperazine (5.1 g) in dry DMF (8 ml) was added. The reaction mixture was heated at 80° C. for 5 hours and then evaporated under reduced pressure. The residue was recrystallised twice to give 1-[2-[4-[(4-fluorophenyl)methyl]-1-piperazinyl]ethyl]-1H-indole-2,3-dione, m.p. 146°-147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05585378 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-09ff7a381dd94e72812a7a24d2a9b4f5 |
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| Source note | uspto-grants-1996_12 |
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