HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 11632828, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 66791198 | HCID 66791198 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11632828 | HCID 11632828 | 99% |
Reaction Steps
Sodium borohydride (1.0 mg, 0.026 mmol), followed by MeOH (0.1 mL), was added to a solution of 4-{2-[(R)-2-oxo-6-((E)-3-oxo-4-phenyl-but-1-enyl)-piperidin-1-yl]-ethylsulfanyl}-butyric acid methyl ester (6.8 mg, 0.017 mmol) in CH2Cl2 (0.3 mL) at 0 ° C. After 15 min at 0° C., the reaction was quenched with aqueous HCl (0.1 M, 4 mL) and extracted with CH2Cl2 (3×5 mL). The combined organic phase was dried (Na2SO4), filtered and concentrated in vacuo to afford 6.8 mg (99%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07435746B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-efce838837e44e1aa803fdc3faa1e985 |
| Source note | uspto-grants-2008_10 |