HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Trityl-1H-imidazole-4-carboxylic acid 4-[4-(3,3-dimethyl-butyryl)-3-hydroxy-2-trifluoromethyl-phenoxymethyl]-benzylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 1-Trityl-1H-imidazole-4-carboxylic acid | HCID 10570117 | — |
| Reactant | 1-[4-(4-Aminomethyl-benzyloxy)-2-hydroxy-3-trifluoromethyl-phenyl]-3,3-dimethyl-butan-1-one hydrochloride | HCID 67176367 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Trityl-1H-imidazole-4-carboxylic acid 4-[4-(3,3-dimethyl-butyryl)-3-hydroxy-2-trifluoromethyl-phenoxymethyl]-benzylamide | HCID 67176101 | 86.7% |
Reaction Steps
Add 1-hydroxybenzotriazole hydrate (63.8 mg; 417 μmol), 1-trityl-1H-imidazole-4-carboxylic acid (148 mg, 417 μmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (79.9 mg, 417 μmol) to anhydrous acetonitrile (7 mL). Stir the reaction mixture at room temperature for 1 hr. Then add 1-[4-(4-aminomethyl-benzyloxy)-2-hydroxy-3-trifluoromethyl-phenyl]-3,3-dimethyl-butan-1-one hydrochloride (150 mg, 347 μmol) and triethylamine (97 μL, 695 μmol). Stir the reaction mixture at room temperature overnight. Quench the reaction with water and the solid, filter the solid and dry to give the title compound (220 mg, 301 μmol). MS (m/z): 730 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754742B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-0b691430937f4d4f8411f80d38d4e078 |
| Source note | uspto-grants-2010_07 |