Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | HCID 86620798 | HCID 86620798 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86620797 | HCID 86620797 | 20% |
Reaction Steps
A solution (15 mL) of 2,2,2-trifluoro-N-({1-[(4-methylphenyl)sulfonyl]-5-phenyl-1H-pyrrol-3-yl}methyl)acetamide (300 mg) in tetrahydrofuran was cooled at 0° C., 1 mol/L tetrahydrofuran solution of borane (2.84 mL) was added, and the mixture was stirred at room temperature for 5 hr and then at 50° C. for 3 hr. Water was added to the reaction mixture, the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→2:1), and the obtained oil was purified by preparative HPLC. The purified product was concentrated under reduced pressure, and the crystals precipitated during the process were collected by filtration. The crystals were recrystallized from ethyl acetate to give the title compound as colorless crystals (yield 70 mg, 20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048909B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-2adfb916df524c0498f7e4ebc7c16e7a |
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| Source note | uspto-grants-2011_11 |
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