Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 71009123 | HCID 71009123 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 71008948 | HCID 71008948 | 96.3% |
Reaction Steps
A solution of (R)-2-methyl-propane-2-sulfinic acid {(R)-1-[1-(3-bromo-phenyl)-1H-pyrazol-4-yl]-2,2-difluoro-3-hydroxy-1-methyl-propyl}-amide (590 mg, 1.2 mmol) in methanol (5 ml) was treated at 0° C. with hydrochloric acid (4N in dioxane, 2.6 ml, 10.2 mmol), and the reaction mixture was stirred at 25° C. for 2 hours. For the workup, the solution was concentrated at reduced pressure, and the resultant residue was diluted with water (10 ml). The aqueous layer was treated with a saturated solution of sodium hydrogencarbonate to a pH of about 8, then extracted with ethyl acetate (4×10 ml). The combined organic layers were washed with brine (15 ml), dried over sodium sulphate, and evaporated at reduced pressure. The crude material thus obtained was purified by column chromatography on silica gel using a gradient of hexane/ethyl acetate=85:15 to 80:20 as the eluent to give the (R)-3-amino-3-[1-(3-bromo-phenyl)-1H-pyrazol-4-yl]-2,2-difluoro-butan-1-ol (400 mg, 96% yield) as a light yellow solid which was used in the next step without further purification. MS (ISP): m/z=346.5 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785436B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-1ac8f84decee4599a70d541a56f107b5 |
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| Source note | uspto-grants-2014_07 |
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