HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 68832620, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57634640 | HCID 57634640 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68832620 | HCID 68832620 | — |
Reaction Steps
To a solution of the exo isomer of ethyl 5-acetyl-2-(4-fluorobenzyl)-3-oxo-2,5-diazabicyclo[4.1.0]heptane-7-carboxylate (3.3 g, 9.87 mmol) in 32 ml EtOH at room temperature was added sodium borohydride (398 mg, 10.5 mmol). After stirring overnight, the reaction mixture was treated with 200 mL MeOH, stirred for 1 h and then concentrated. The residue was dissolved in dichloromethane (100 mL), treated with 1N HCl (10 mL) and water (20 mL). The aqueous phase was back extracted with chloroform (2×50 mL). The combined organic phases were dried over sodium sulfate, filtered and concentrated. The residue was purified by column chromatography on silica gel using ethyl acetate and methanol as eluents to give title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517532B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-73d8250ba54e442aba29a402153d4d67 |
| Source note | uspto-grants-2009_04 |