Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-Hydroxy-2-(4-{4-[6-(6-trifluoromethyl-pyridin-3-ylamino)-pyridazin-3-yl)-phenyl}-cyclohexyl)-acetamidine | HCID 178510747 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 136365348 | HCID 136365348 | — |
Reaction Steps
To a solution of N-Hydroxy-2-(4-{4-[6-(6-trifluoromethyl-pyridin-3-ylamino)-pyridazin-3-yl]-phenyl}-cyclohexyl)-acetamidine (0.13 g, 0.28 mmol, 1.0 equiv) in 2 Ml DMF was added pyridine (0.023 Ml, 0.31 mmol, 1:1 equiv). The solution was cooled to 0° C., then isobutyl chloroformate (0.04 Ml, 0.31 mmol, 1.1 equiv) was added dropwise via syringe. The reaction was allowed to warm to room temperature and stirred for 2 h. Extractive aqueous workup afforded the title compound which was used in the next step without further purification. (M+H)+571.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835451B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-b3183dfde2ff4501a65caf3b57aa55c5 |
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| Source note | uspto-grants-2014_09 |
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