Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 71610191 | HCID 71610191 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71610222 | HCID 71610222 | 56% |
Reaction Steps
A mixture of Example 64 (110 mg; 0.25 mmol; 1 eq.), acetone (109 μL; 1.49 mmol; 6 eq.) and sodium triacetoxyborohydride (210 mg; 0.99 mmol; 4 eq.) in DCM (6 mL) was stirred at room temperature for 60 hours. The reaction mixture was diluted with DCM, washed with sat. aq. NaHCO3, dried over sodium sulfate and concentrated in vacuo. Purification by mass directed preparative HPLC afforded the title compound (68 mg, 56%) as a yellow powder. 1H NMR (CDCl3) δ 7.33 (td, J=8.2, 6.7 Hz, 1H), 6.80-6.63 (m, 2H), 5.05-4.91 (m, 2H), 4.67 (br s, 2H), 4.36 (br s, 1H), 2.91 (s, 2H), 2.86 (s, 1H), 2.78-0.52 (m, 6H), 2.46-2.24 (m, 2H), 2.06-1.88 (m, 2H), 1.88-1.70 (m, 2H), 0.94 (d, J=6.5 Hz, 6H). HPLC (max plot) 94.1%, Rt 3.02 min. UPLC/MS: (MS+) 486.5 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09403835B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-4c19052352324263b0b455142f8d5615 |
|---|
| Source note | uspto-grants-2016_08 |
|---|