HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 57741529, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 66621762 | HCID 66621762 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57741529 | HCID 57741529 | 69.4% |
Reaction Steps
Treat a solution of chiral 1-cyclohexyl-3-[3,5-dichloro-4′-(2,5-diaza-bicyclo[2.2.1]heptane-2-carbonyl)-biphenyl-4-ylmethyl]-pyrrolidin-2-one (0.096 g, 0.18 mmol) in methanol (3 mL) and acetone (0.105 g, 1.81 mmol) with sodium cyanoborohydride (0.055 g, 0.88 mmol) and then acetic acid (0.057 g, 0.94 mmol). Stir the mixture for 3 hours at room temperature under a nitrogen atmosphere, dilute with ethyl acetate and wash with saturated sodium bicarbonate then water. Dry the organic layer with sodium sulfate and purify the crude product by silica gel chromatography using a gradient of 0 to 10% methanol in dichloromethane to afford 71 mg (68%) of the title compound: MS (m/z): 568 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088776B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-8dbb80cfd92e48f7ae82e694b25e8dcd |
| Source note | uspto-grants-2012_01 |