HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 59170971, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59170865 | HCID 59170865 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59170971 | HCID 59170971 | 10.5% |
Reaction Steps
Sodium borohydride (2 mg) is added to an ethanol (1 mL) solution of (E)-3-(3-formyl-4-(1H-imidazol-1-yl)phenyl)-N-indan-1-ylacrylamide (17 mg) obtained in Example 437 and the reaction mixture was agitated for 30 minutes at room temperature. After the reaction solution was concentrated under reduced pressure, water and ethyl acetate were added to the residue, and the organic layer was partitioned. The organic layer was washed with a saturated saline solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Carrier: Chromatorex™ NH, elution solvent:methanol-ethyl acetate system), and 1.8 mg of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07667041B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-dbb0c375bd7945bfb258f48036acfeb7 |
| Source note | uspto-grants-2010_02 |