Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazin-2-one | HCID 231360 | — |
| Reactant | 2-[4-(p-Chlorophenyl)-2-oxopyrrolidin-1-yl]-acetic acid pentachlorophenyl ester | HCID 53974966 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Cebaracetam | HCID 65919 | — |
Reaction Steps
4.46 g (44.6 mmol) of piperazin-2-one (ketopiperazine) and 300 ml of dimethylformamide are added to 22.4 g (44.6 mmol) of 2-[4-(p-chlorophenyl)-2-oxopyrrolidin-1-yl]-acetic acid pentachlorophenyl ester and the whole is stirred for 5 hours at room temperature. The whole is concentrated to dryness by evaporation under reduced pressure at 70°, stirred with 150 ml of ethyl acetate for 1 hour and then 150 ml of diethyl ether are added; the whole is filtered with suction, washed with 50 ml of diethyl ether and allowed to dry. 1-[4-(p-chlorophenyl)-2-oxopyrrolidin-1-ylacetyl]-3-oxopiperazine having a melting point of 205°-207° is obtained and can be purified further by recrystallisation from 300 ml of butanol, washing with 50 ml of diethyl ether and drying, and then melts at 208°-210°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04945092 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-58d1f6c818ee4bbca9ca27645de879eb |
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| Source note | uspto-grants-1990_07 |
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