Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Cyclopropylacetylene | HCID 138823 | — |
| Reactant | HCID 86653109 | HCID 86653109 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86653116 | HCID 86653116 | 84.6% |
Reaction Steps
To a stirred solution of N-[(2,5-dichloro-1,3-thiazol-4-yl)methoxy]-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimine (0.15 g, 0.406 mmol, 1 eq.) in 3 ml dry THF “degassed” with N2, was added Cyclopropylacetylene (0.029 g, 0.447 mmol, 1.1 eq.) followed by N-ethyldiisopropylamine (0.209 g, 1.62 mmol, 4 eq.), Copper Iodide (0.015 g, 0.081 mmol, 0.2 eq.) and Tetrakis(triphenylphosphine)palladium (0.046 g, 0.041 mmol, 0.1 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-{[5-chloro-2-(cyclopropylethynyl)-1,3-thiazol-4-yl]methoxy}-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimine (0.137 g, 71% yield, 78:5 mixture of stereoisomers) as a yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466176B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-c47d7eae18074afdbc7cc9a09684770c |
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| Source note | uspto-grants-2013_06 |
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