HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (S)-2-[[(S)-2-(4-Hydroxy-1-oxobutyl)-1-pyrrolidinyl]carbonyl]-N-(phenylmethyl)-1-pyrrolidinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzyl isocyanate | HCID 76639 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | (S)-1-(tert-Butoxycarbonyl)-2-[1-hydroxy-4-(phenylmethyloxy)butyl]pyrrolidine | HCID 67745428 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (S)-2-[[(S)-2-(4-Hydroxy-1-oxobutyl)-1-pyrrolidinyl]carbonyl]-N-(phenylmethyl)-1-pyrrolidinecarboxamide | HCID 54373947 | 77.9% |
Reaction Steps
4N Hydrochloric acid (1,4-dioxane solution, 20 ml) was added to (S)-1-(tert-butoxycarbonyl)-2-[1-hydroxy-4(phenylmethyloxy)butyl]pyrrolidine (high polar isomer, 3.00 g) and the mixture was allowed to stand at room temperature for 30 minutes. The reaction mixture was concentrated and the residue was reacted with N-(benzylamincarbonyl)-L-proline obtained by stirring L-proline (0.99 g), benzyl isocyanate (0.97 g) and triethylamine (0.87 g) in DMF (10 ml) at room temperature for 1 hour, in the same manner as in Example 5-b), to give the title compound (2.20 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05536737 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-1ad2442966b24a8d9d95dcbb32e1e2eb |
| Source note | uspto-grants-1996_07 |