Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Cyclopropylacetylene | HCID 138823 | — |
| Reactant | HCID 86650769 | HCID 86650769 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86650770 | HCID 86650770 | 190.3% |
Reaction Steps
To a stirred solution of N-[(6-bromopyridin-2-yl)methoxy]-1-(4-methyl-4H-1,2,4-triazol-3-yl)-1-phenylmethanimine (0.125 g, 0.33 mmol, 1 eq.) in 3 ml dry THF “degassed” with N2, was added Cyclopropylacetylene (0.95 g, 0.1 mmol, 3 eq.) followed by N-ethyldiisopropylamine (0.216 g, 1.67 mmol, 5 eq.), Copper Iodide (0.012 g, 0.06 mmol, 0.2 eq.) and Tetrakis(triphenylphosphine)palladium (0.077 g, 0.06 mmol, 0.2 eq.). The reaction was microwaved 120° C./normal/fixed hold/pre stir 100 s for 180 s. The reaction was diluted with EtOAc and filtered through a “celite” plug. The solvent was evaporated and the residue purified by chromatography on silica gel to give N-{[6-(cyclopropylethynyl)pyridin-2-yl]methoxy}-1-(4-methyl-4H-1,2,4-triazol-3-yl)-1-phenylmethanimine (0.068 g, 56% yield) as a yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08981111B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-ab2f82e3138f4feba5a9351e0c109968 |
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| Source note | uspto-grants-2015_03 |
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