Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Aminobenzoic Acid | HCID 978 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 4-Benzylpiperidine | HCID 31738 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18616321 | HCID 18616321 | 51.8% |
Reaction Steps
4-Aminobenzoic acid (1.61g, 10 mM) was reacted with EDAC (1.92g, 10 mM) in 40 mL dry DMF for 15 minutes. 4-Benzylpiperidine (1.75g, 10 mM) was added followed by DMAP (20 mg, catalyst) and the reaction mixture was stirred for 20 h. The mixture was poured into water and extracted with methylene chloride (3×100 mL). The combined extract was washed with dilute hydrochloric acid, saturated sodium bicarbonate and water and dried over MgSO4. After evaporation of the solvent, the residue was chromatographed with methylene chloride-methanol (0 to 2% methanol, gradient) to yield 1.60 g (50%) of the title compound after recrystallization from ether-Hexane. 1H NMR (CDCl3): δ 7.40-7.10 (m, 7H), 6.70 (d, 2H), 3.95-3.90 (broad m, 2H), 2.85-2.75 (broad m, 2H), 2.6 (d, 2H), 1.85-1.80 (m, 1H), 2.75-2.65 (broad m, 2H), 1.15-1.05 (broad m, 2H). MS (ESI) m/e 294 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06541477B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-7a418637f1954e9094a10593d1a7ff14 |
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| Source note | uspto-grants-2003_04 |
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