Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid | HCID 392871 | — |
| Reactant | 2-Bromo-4-isopropylaniline | HCID 521337 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58878501 | HCID 58878501 | — |
Reaction Steps
Piperidine-1,4-dicarboxylic acid mono-tert-butyl ester (2.97 g, 13 mmol) was dissolved in dry methylene chloride (25 mL) and dry pyridine (2.7 mL). To the reaction mixture was then added thionyl chloride (1.86 g, 15.6 mmol) under nitrogen atmosphere and the reaction mixture was stirred at room temperature for 30 minutes. To the reaction mixture was then added successively, under nitrogen atmosphere, 2-bromo-4-isopropyl-phenylamine (3.0 g, 14 mmol), dry triethylamine (4.6 g, 45.5 mmol), dry methylene chloride (20 mL), 4-(dimethylamino)pyridine (0.16 g, 1.3 mmol) and the reaction mixture was stirred at room temperature for 24 hours. The reaction mixture was then partitioned with aqueous 2N HCl and tert-Butyl methyl ether. The organic layer was washed with aqueous 2N HCl, aqueous NaHCO3, brine, dried with Na2SO4, filtered and the solvent evaporated in vacuo to yield a crude oil. The crude oil was recrystallized from ethyl acetate/hexanes to yield the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07655670B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-8e6e4b01571d4085839358402afce777 |
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| Source note | uspto-grants-2010_02 |
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