Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 66616568 | HCID 66616568 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | dichloromethane N,N-dimethylformamide | HCID 22350042 | — |
| Product | HCID 66616612 | HCID 66616612 | 105.1% |
Reaction Steps
To a solution of 4′-fluoro-5-(methoxycarbonyl)biphenyl-3-carboxylic acid (400 mg, 1.459 mmol) in DMF/CH2Cl2 at rt was added EDCI.HCl (363 mg, 1.896 mmol) followed by HOBt.H2O (197 mg, 1.459 mmol). After one minute, (4-fluorophenyl)methanamine (183 mg, 1.459 mmol) was added to the mixture and the reaction mixture was stirred at rt for 4 h. To the reaction mixture were added EtOAc and aq. NaHCO3. The EtOAc layer was separated, washed with water, dried over MgSO4 and concentrated in vacuo to obtain a crude product as a light yellow solid (585 mg, >100% yield), MS: M+H=382.21. The crude product was used directly in the next step without further purification. 1H NMR (CDCl3): δ 8.39 (s, 1H), 8.32 (s, 1H), 7.58˜7.02 (m, 9H), 4.63 (d, J=6.0 Hz, 2H), 3.95 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501992B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-467034407867456dbe04df494c32b000 |
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| Source note | uspto-grants-2013_08 |
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