Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyl 4-(4-cyano-2-fluorophenyl)piperazine-1-carboxylate | HCID 53485511 | — |
| Reactant | HCID 178478989 | HCID 178478989 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 69303640 | HCID 69303640 | — |
Reaction Steps
A −78° C. solution of 4-(4-cyano-2-fluoro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (0.27 g, 0.87 mmol) in Et2O (10 mL) was treated with cyclopentylmagnesium chloride (1.5 mL, 2 M). The mixture was allowed to slowly reach rt overnight. The reaction was then cooled to 0° C. and water added (10 mL). The pH of the mixture was adjusted to ˜7 with 1 M HCl and was extracted with Et2O and the solvent removed. Purification on SiO2EtOAc/hexanes) provided 0.19 g of the title compound. MS (ESI): mass calcd. for C21H29FN2O3, 376.47. m/z found, 377.5 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183239B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-720e4e6b38e740b6aba1f48a65ccc119 |
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| Source note | uspto-grants-2012_05 |
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