HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 86222010, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | HCID 18457814 | HCID 18457814 | — |
| Product | HCID 86222010 | HCID 86222010 | — |
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 cyclopropylamine (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′-cyclopropyl-6-methyl-N3-propyl-1,1′-biphenyl-3,4′-dicarboxamide. NMR: δH CDCl3 7.79, (2H, d), 7.67, (1H, dd), 7.60, (1H, d), 7.32, (3H, m), 6.56, (1H, s), 6.35, (1H, t), 3.41, (2H, q), 2.92, (1H, m), 2.25, (3H, s), 1.63, (2H, m), 0.97, (3H, t), 0.88, (2H, m), 0.65, (2H, m). LCMS: retention time 2.95 min, MH+337.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07208629B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-7d600b76f3a8422f946234b881824d35 |
| Source note | uspto-grants-2007_04 |