HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 22506963, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22506968 | HCID 22506968 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22506963 | HCID 22506963 | 69.3% |
Reaction Steps
A suspension was prepared of 6-[2-(4-chloro-phenyl)-2-oxo-ethanesulfonyl]-2H-pyridazin-3-one (1.0 mmol, 312 mg) prepared according to Example 18 in methanol (10 mL). Sodium borohydride (1.5 mmol, 55 mg) was added to the suspension at room temperature and stirred for 1 hour. The reaction mixture was evaporated and the residue was triturated with 10% hydrochloric acid (5 mL). The resulting white precipitate was filtered and air-dried to afford the title compound (69%, 218 mg); mp, 178-179° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06872722B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-c447d8bd9d5a49fbaeb9a2f021518856 |
| Source note | uspto-grants-2005_03 |