HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 68564972, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Phthalimide, N-(2-formylethyl)- | HCID 75525 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 45588680 | HCID 45588680 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68564972 | HCID 68564972 | — |
Reaction Steps
To a solution of 1-(1-benzyl-1H-benzimidazol-2-yl)-2-methyl-propylamine (160 mg, 0.56 mmol) and 3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionaldehyde (114 mg, 0.56 mmol) in dry DCM (3 ml) at room temperature, was added sodium triacetoxyborohydride (119 mg, 0.56 mmol). After 10 minutes, acetic acid (34 μl, 0.56 mmol) was added to the reaction mixture. The mixture was stirred at room temperature for 1 hour. The solvent was removed in vacuo and the solid was dissolved in ethyl acetate. The organic layer was washed with saturated NaHCO3, dried over MgSO4, filtered and the filtrate was concentrated in vacuo. The crude product was purified by flash chromatography to give material that was used in Example 5g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662581B1 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-1e1e979e48404e939c081ca120585047 |
| Source note | uspto-grants-2010_02 |