Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cyclopropanemethanamine | HCID 75646 | — |
| Reactant | HCID 18457814 | HCID 18457814 | — |
| Product | HCID 44578844 | HCID 44578844 | — |
Reaction Steps
5′-[(1H-1,2,3-Benzotriazol-1-yl)carbonyl]-2′-methyl-N-propyl-1,1′-biphenyl-3-carboxamide (25 mg, 0.062 mmol) in THF (1 ml) was mixed with cyclopropylmethylamine (7.2 μl) in THF (0.6 ml) and the reaction stirred at room temperature for 4 h. The reaction was loaded onto an SPE (aminopropyl, 1 g) and eluted with chloroform, ethyl acetate and methanol. The solvent was evaporated from the product fractions to give N4′-cyclopropylmethyl-6-methyl-N3-propyl-1,1′-biphenyl-3,4′-dicarboxamide. NMR: δH CDCl3 7.84, (2H, d), 7.68, (1H, dd), 7.62, (1H, d), 7.38, (2H, d), 7.33, (1H, d), 6.37, (1H, t), 6.26, (1H, t), 3.42, (2H, m), 3.35, (2H, m), 2.28, (3H, s), 1.64, (2H, m), 1.09, (1H, m), 0.98, (3H, t), 0.58, (2H, m), 0.30, (2H, m). LCMS: retention time 3.13 min, MH+351.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208629B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-761c1c785d6d4f5dacbd90e5dd92c606 |
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| Source note | uspto-grants-2007_04 |
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