Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | 1-(2-Tert-butylphenyl)piperazine dihydrochloride | HCID 66751149 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66792770 | HCID 66792770 | — |
Reaction Steps
A mixture of 1-(2-tert-butylphenyl)piperazine dihydrochloride obtained in Reference Example 1 (1.00 g, 3.42 mmol), 4-nitrobenzoyl chloride (0.761 g, 4.1 mmol) and triethylamine (1.67 mL, 12.0 mmol) in tetrahydrofuran (25 mL) was stirred at room temperature for overnight. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give a solid. A mixture of the obtained solid and 10% of palladium-carbon (100 mg) in tetrahydrofuran (30 mL) and methanol (100 mL) was stirred at room temperature under hydrogen atmosphere (5 atm). After being stirred for 3 h, the reaction mixture was filtrated and concentrated to purify the residue by NH-silica gel column chromatography (hexane/ethyl acetate 0:100) and the title compound was obtained as a solid (1.28 g, quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853215B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-a5ae6296a1c04d2f8bf237da24b118e5 |
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| Source note | uspto-grants-2014_10 |
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