Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | tert-Butyl 2-methylpiperazine-1-carboxylate | HCID 15087784 | — |
| Reactant | N-(4-Chlorobutyl)-N-(4-fluorophenyl)-3-pyridinecarboxamide | HCID 15087790 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15087792 | HCID 15087792 | 57.2% |
Reaction Steps
A mixture of 5 parts of N-(4-chlorobutyl)-N-(4-fluorophenyl)-3-pyridinecarboxamide, 2.77 parts of (1,1-dimethylethyl) 2-methyl-1-piperazinecarboxylate, 1.58 parts of sodium carbonate and 94 parts of N,N-dimethylformamide was stirred for 48 hours at 90° C. The reaction mixture was evaporated and the residue was taken up in water. The product was extracted twice with dichloromethane. The combined extracts were washed with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (96:4 by volume) as eluent. The first fraction was collected and the eluent was evaporated, yielding 3.5 parts (57.2%) of (1,1-dimethylethyl) 4-[4-[[4-fluorophenyl)(3-pyridinylcarbonyl)amino]butyl]-2-methyl-1-piperazinecarboxylate as a residue (int. 43).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05026853 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-6b09118d4d864cd781393aed1b007e29 |
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| Source note | uspto-grants-1991_06 |
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