HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 57429280, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57429279 | HCID 57429279 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57429280 | HCID 57429280 | — |
Reaction Steps
To a suspension of 1-(methylthio)-6,7-dihydro-8H-pyrido[3,4-b]pyrrolizin-8-one from Example 6 method-1 Step 5 (0.55 g, 2.2 mmol) in EtOH (10 mL)-TH (1 mL) was added NaBH4 (0.10 g, 2.6 mmol) at 0° C. After a period of 30 min. at room temperature, the reaction was quenched by the addition of acetone. The solvents were evaporated under reduced pressure and EtOAC and H2O were added to the residue. The organic phase was separated, dried over MgSO4 and evaporated. The title compound was washed with EtOAc/Hexane and filtered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618979B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-59c3d7625a9f483cafc5315667b8e631 |
| Source note | uspto-grants-2009_11 |