HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → N-(2-hydroxy-ethyl)-2-[2-(4-trifluoromethyl-phenoxymethyl)-1H-benzoimidazol-5-yl]-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 2-[2-(4-trifluoromethyl-phenoxymethyl)-1H-benzoimidazol-5-yl]-benzoic acid | HCID 178524279 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-hydroxy-ethyl)-2-[2-(4-trifluoromethyl-phenoxymethyl)-1H-benzoimidazol-5-yl]-benzamide | HCID 178523439 | 78% |
Reaction Steps
A mixture of 2-[2-(4-trifluoromethyl-phenoxymethyl)-1H-benzoimidazol-5-yl]-benzoic acid (0.050 g, 0.121 mmol), BOP (0.059 g, 0.133 mmol), DIPEA (0.07 mL, 0.363 mmol) and ethanolamine (0.011 g, 0.182 mmol) in DMF (0.5 mL) was stirred at rt for 12 hours. The crude product was purified by chromatography (silica, CH2Cl2: MeOH, 5:1) to afford the title compound as a brown oil (0.043 g, 78%). 1H NMR (400 MHz, CD3OD) δ (ppm): 7.64-7.59 (m, 3H), 7.54-7.46 (m, 4H), 7.41 (td, 1H, J=8.2 Hz, J=1.6 Hz), 7.35 (dd, 1H, J=8.0 Hz, J=1.6 Hz), 7.15 (d, 2H, J=8.0 Hz), 5.42 (s, 2H), 5.24 (s, 1H), 3.91 (t, 2H, J=6.0 Hz), 3.24 (t, 2H, J=6.2 Hz). Mass Spectrum (LCMS, ESI pos.) Calcd. For C24H21F3N3O3: 456.4 (M+H), Found 456.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612211B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-c7b94cf407ab4d61b5dd56dbd8d9228a |
| Source note | uspto-grants-2009_11 |