HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → (S)-1-(benzyloxycarbonyl)-3-(N,N-diethylamino)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (S)-1-Cbz-3-Aminopyrrolidine | HCID 1519355 | — |
| Product | (S)-1-(benzyloxycarbonyl)-3-(N,N-diethylamino)pyrrolidine | HCID 68693001 | — |
Reaction Steps
To a solution of 1.40 g of (S)-3-amino-1-(benzyloxycarbonyl)pyrrolidine (J. Med. Chem., 1992, 35, 1764-1773) in 28 ml of tetrahydrofuran, 2.6 g of potassium carbonate and 1.0 ml of ethyl iodide were added under ice-cool stirring, followed by stirring for 24 hours. The reaction solution was concentrated under reduced pressure, mixed with water, followed by extraction with ethyl acetate, and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 0.70 g of the objective compound as a yellow oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728131B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-2f4d393ee06c4c96bd870b37c357c585 |
| Source note | uspto-grants-2010_06 |