Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(2-Methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-ol | HCID 21911691 | — |
| Reactant | 3-Chloro-1-phenylpyrrolidin-2-one | HCID 21935559 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11271280 | HCID 11271280 | — |
Reaction Steps
To a solution of 3-chloro-1-phenylpyrrolidin-2-one (100 mg, 0.51 mmol) in EtOH (10 mL) was added 1-(2-methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-ol as prepared in Example 3A (190 mg, 0.62 mmol) and Et3N (0.2 mL, 1.43 mmol). The solution was stirred at 85° C. for 60 hours. Upon cooling, the solution was concentrated to an oil and purified via flash column chromatography to afford 3-{4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinyl}-1-phenylpyrrolidin-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262198B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-dd86d7c8da544fdab19674c119f12a77 |
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| Source note | uspto-grants-2007_08 |
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