HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 89876292, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 89876303 | HCID 89876303 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 89876292 | HCID 89876292 | 75.2% |
Reaction Steps
To a stirred solution of 6-acetyl-4-(2,3-dichloroindol-1-yl)-5-methoxy-2-methyl-pyridazin-3-one (500 mg, 1.37 mmol) in ethanol (1 mL) at 0° C. is added sodium borohydride (79 mg, 2.05 mmol). After stirring for 20 min, the reaction is quenched with water (10 mL), then concentrated under reduced pressure to remove most of the ethanol. The aqueous solution is then extracted with Et2O (20 mL×2), then concentrated under reduced pressure to give the desired product 4-(2,3-dichloroindol-1-yl)-6-(1-hydroxyethyl)-5-methoxy-2-methyl-pyridazin-3-one (379 mg, 1.03 mmol, 75%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09049864B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-4bdf3cb1509349539fb7f9fe5c0e1d02 |
| Source note | uspto-grants-2015_06 |