Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | HCID 59238302 | HCID 59238302 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59238276 | HCID 59238276 | — |
Reaction Steps
To a solution of (E)-2-{4-[2-(2-tert-butoxycarbonylamino-phenylcarbamoyl)-vinyl]-phenyl}-4-(1-methyl-pyrrolidin-2-yl)-butyric acid (2.54 g, 5 mmol), Et3N (1.21 g, 10 mmol), and HATU (3.80 g, 10 mmol) in CH2Cl2 (30 mL) was added 4-bromo-phenylamine (1.29 g, 7.5 mmol). This mixture was stirred overnight at room temperature and then evaporated. The mixture redissolved in 20 mL of EtOAc and washed with 2N HCl (20 mL×3), brine, 5% NaHCO3 (20 mL×3), brine, dried with Na2SO4, filtered and evaporated. The residue was purified by column chromatography on silica gel using hexane/EtOAc to give a white solid. 1.25 M HCl/MeOH (4 mL) was added to the product. The solution was stirred for 4 h at ambient temperature. After reaction, the solution was neutralized with solid NaHCO3. The final product was obtained by preparative HPLC. MS: calc'd 561 (MH+), exp 561 (MH+). 1H NMR (d6-DMSO, 400 MHz), 10.25 (d, 1H, J=8.8 Hz), 9.40 (s, 1H), 7.60-7.56 (m, 4H), 7.53 (d, 1H, J=15.6 Hz), 7.49-7.45 (m, 4H), 7.34 (d, 1H, J=8.0 Hz), 6.93 (d, 1H, J=7.6 Hz), 6.88 (d, 1H, J=15.6 Hz), 6.75 (d, 1H, J=7.6 Hz), 6.58 (t, 1H, J=8.0 Hz), 4.95 (s, 2H), 3.71 (broad s, 1H), 3.07 (broad s, 1H), 2.31 (broad s, 4H), 1.99 (broad s, 2H), 1.69-1.46 (broad m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202866B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-e38872ae4d66410e8b3040d99efacaa8 |
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| Source note | uspto-grants-2012_06 |
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