Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 23092434 | HCID 23092434 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23092424 | HCID 23092424 | — |
Reaction Steps
3-tert-Butoxycarbonylamino-2,6-dimethyl-4-trifluoromethylpyridine(21.12 g, 72.8 mmol) was dissolved in methanol (70 mL). 10% hydrochloric acid in methanol (140 mL) was added to the solution, followed by stirring for 12 hours at 60° C. The reaction mixture was concentrated under reduced pressure, and the residue was suspended in a solvent mixture of ethyl acetate-ether, followed by collection through filtration and washing with ether, to thereby yield 3-amino-2,6-dimethyl-4-trifluoromethylpyridine dihydrochloride as a colorless powder (15.64 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07459552B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-4ab2be1446d4467fae67579971758a75 |
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| Source note | uspto-grants-2008_12 |
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