Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piconol | HCID 11474 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | HCID 86616995 | HCID 86616995 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86616994 | HCID 86616994 | 47.1% |
Reaction Steps
To a solution of tert-butyl (1R)-1-(5-{3-chloro-6-((2-methoxyethyl){[trans-2-methylcyclopropyl]methyl}amino)-2-[(methylsulfonyl)amino]pyridin-4-yl}-1,3,4-oxadiazol-2-yl)-1-methyl-2-phenylethylcarbamate (intermediate 8.4.2, 0.028 g, 0.043 mmol) in toluene (1 ml) at 0 oC was added 2-(hydroxymethyl)pyridine (0.004 ml, 0.043 mmol) and triphenylphosphine (0.011 g, 0.043 mmol) followed by diisopropyl azodicarboxylate (0.008 ml, 0.043 mmol). The ice bath was removed and the solution stirred at room temperature overnight. The next day the solution was concentrated in vacuo, taken up in DMF and filtered. The product was purified by reverse phase HPLC affording 0.015 g of tert-butyl (1R)-1-(5-{3-chloro-6-((2-methoxyethyl){[trans-2-methylcyclopropyl]methyl}amino)-2[(methylsulfonyl)(pyridin-2-ylmethyl)amino]pyridin-4-yl}-1,3,4-oxadiazol-2-yl)-1-methyl-2-phenylethylcarbamate LCMS [M+H]740.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394837B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-9cfae98c36ce42b2a000ddb7f6510125 |
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| Source note | uspto-grants-2013_03 |
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