Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-methyl-1H-imidazole-4-carboxylic acid | HCID 541509 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 67177680 | HCID 67177680 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59153165 | HCID 59153165 | 53.4% |
Reaction Steps
Mix 1-[4-(4-aminomethyl-benzyloxy)-2-hydroxy-3-trifluoromethyl-phenyl]-3-methyl-butan-1-one hydrochloride (120 mg, 287.2 μmol), 1-methyl-1-H-imidazole-4-carboxylic acid (43.5 mg, 344.6 μmol), 1-hydroxybenzotriazole hydrate (52.8 mg, 344.6 μmol) in anhydrous tetrahydrofuran (4.5 mL). Add triethylamine (72.7 mg, 718 μmol, 100 μL) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (66.1 mg, 344.6 μmol) to the mixture. Stir the reaction mixture at room temperature overnight. Dilute the reaction mixture with water. Extract the mixture with ethyl acetate (3×). Combine the organic layers, wash with brine, dry over sodium sulfate, and concentrate under reduced pressure. Purify the crude residue by flash chromatography (silica gel) eluting with 5% methanol/ethyl acetate followed by reverse phase chromatography using 90/10 to 20/80 (water/0.1% trifluoroacetic acid)/acetonitrile to provide the product as a white solid (75 mg, 153 μmol, 53.4% yield). MS (m/z): 490 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754742B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-2ef13e3830df41fea16e3aa92630bece |
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| Source note | uspto-grants-2010_07 |
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