Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 23092434 | HCID 23092434 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23092424 | HCID 23092424 | 82% |
Reaction Steps
3-tert-Butoxycarbonylamino-2,6-dimethyl-4-trifluoromethylpyridine (21.12 g, 72.8 mmol) was dissolved in methanol (70 mL), and subsequent to the addition of 10% hydrogen chloride in methanol (140 mL), the solution was stirred at 60° C. for 12 hours. The reaction mixture was concentrated under reduced pressure, and the residue was suspended in a mixture of ethyl acetate and ether. The reaction product was collected by filtration, and washed with ether to obtain the title compound (15.64 g, 82%) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750150B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-8928bfea98854ac699cb90f9e2f450d5 |
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| Source note | uspto-grants-2010_07 |
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