Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 69035635 | HCID 69035635 | — |
| Catalyst | Acetone | HCID 180 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69039943 | HCID 69039943 | 58% |
Reaction Steps
A mixture of 39h-b (170 mg, 300 μmol), acetone (871 μL, 11.9 μmol), acetic acid (69.1 μL, 1.20 mmol), and sodium triacetoxyborohydride (255 mg, 1.20 mmol) in dichloroethane (17 mL) was stirred at room temperature for 2 h. The reaction was diluted with EtOAc (500 mL), washed with saturated NaHCO3 (3×150 mL), water (2×100 mL), and brine (150 mL), dried over Na2SO4, filtered, and evaporated. The residue was purified by CombiFlash chromatography (silica, 0–10% MeOH/CH2Cl2) to provide (R*)-1-((1S*,2R*,4R*)-4-(isopropylamino)-2-(phenylsulfonylmethyl)cyclohexyl)-3-((2-(3-(trifluoromethyl)phenyl)-1,3-dioxolan-2-yl)methyl)pyrrolidin-2-one (39i-b, 106 mg, 58%) as a white solid: 1H NMR (300 MHz, CDCl3) δ 7.89 (d, J=7.2 Hz, 2H), 7.68 (s, 1H), 7.64–7.39 (m, 6H), 4.20 (s, 1H), 4.05–3.90 (m, 2H), 3.81–3.60 (m, 3H), 3.48–3.11 (m, 4H), 3.10–2.88 (m, 1H), 2.60–2.10 (m, 5H), 2.09–1.60 (m, 8H), 1.43–1.00 (m, 6H); 19F NMR (282 MHz, CDCl3) δ −62.9; ESI MS m/z 609 [C31H39F3N2O5S+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183270B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-74b177bc21464446914e0f523caf6601 |
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| Source note | uspto-grants-2007_02 |
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