HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → methyl 2-[(3S)-1-Cbz-3-pyrolidinyl(cyclohexyl)amino]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | HCID 67343263 | HCID 67343263 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 2-[(3S)-1-Cbz-3-pyrolidinyl(cyclohexyl)amino]acetate | HCID 67379348 | 90% |
Reaction Steps
NaH (60% in mineral oil, 52.0 mg, 1.30 mmol) was placed in a round-bottom flask, filled with nitrogen, and then THF (10 mL) was added. A solution of (3S)-1-Cbz-3-(cyclohexylamino)pyrrolidine (302 mg, 1.00 mmol) prepared in Intermediate 2 in THF was added dropwise at 0° C., and the reaction mixture was stirred for 30 min until no further gas evolution occurred, followed by slow addition of methyl bromoacetate. After 4 h, the reaction, mixture was quenched with water and extracted with EtOAc. The extracts were dried over MgSO4 and concentrated in vacuo, and the residue was purified by column chomatography (EtOAc/Hex=1/2) to give the title compound (227 mg, 90.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989634B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-10f4142bf1eb43fcb524c8da4d5962f8 |
| Source note | uspto-grants-2011_08 |