Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-(Bromomethyl)-3-chlorobenzene | HCID 69838 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 4-Acetyl-2-piperazinone | HCID 12744517 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54684774 | HCID 54684774 | — |
Reaction Steps
To a cold (0° C.) solution of 4-acetylpiperazin-2-one (1.0 g, 7.0 mmol) in DMF (75 mL) under an atmosphere of nitrogen, a solution of lithium bis(trimethylsilyl)-amide in THF (7.7 mL, 7.7 mmol) was added and stirred at the temperature for 30 min. The resultant solution was treated with 3-chlorobenzyl bromide (0.92 mL, 7.0 mmol), and stirred at room temperature overnight. The resultant mixture was cooled to 0° C., treated with a solution of lithium bis(trimethylsilyl)amide in THF (8.4 mL, 8.4 mmol) and stirred for 30 min, and then treated with diethyl oxalate (0.96 mL, 7.0 mmol). The resultant mixture was stirred at room temperature overnight. Additional solution of lithium bis(trimethylsilyl)amide in THF (16.8 mL, 16.8 mmol) was added and stirred for 4 hrs. The product mixture was concentrated under vacuum, and the residue was treated with a mixture of aqueous HCl and ethyl acetate. The white solid precipitated was collected by filtration and was subjected to HPLC purification on C-18 stationary phase eluted with water/acetonitrile/TFA mobile phase. Collection and lyophilization of appropriate fractions provided the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517532B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-c9e79b274c7f4a32a66f9ba2365b86b2 |
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| Source note | uspto-grants-2009_04 |
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