Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | HCID 68089001 | HCID 68089001 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 68089119 | HCID 68089119 | 28% |
Reaction Steps
An 8 mL vial is charged with acetonitrile (0.5 mL), 5-(6-ethoxyimidazo[2,1-f]pyridazin-2-yl)-2-(trifluoromethyl)benzoic acid (0.035 g, 0.0001 mol), tert-butylamine (0.016 mL), triethylamine (0.055 mL), and (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (0.088 g). The mixture is stirred and heated at 80° C. for 16 hr, cooled, concentrated onto celite and purified by silica (0-100% EtOAc in Hexanes) to give the title compound (0.011 g, 28% yield). LCMS m/z=407.5 [M+H]+, tR=2.74 min. (compound same as Example 211)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871767B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-48e034b6cf7e4ab6a410dc800cb1dd56 |
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| Source note | uspto-grants-2014_10 |
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