HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(N-benzyloxycarbonyl-2(S)-aminobutyryl)-L-proline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (2S)-2-(((Phenylmethoxy)carbonyl)amino)butanoic acid | HCID 7349998 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 1-(N-benzyloxycarbonyl-2(S)-aminobutyryl)-L-proline | HCID 21344934 | — |
Reaction Steps
A solution of 2.1395 g of L-proline (18.6 mmol) and 1.56 g of NaHCO3 (18.6 mmol) in water (20 ml) is treated with a solution of 4.138 g of the succinimide ester of N-benzyloxycarbonyl-2(S)-aminobutyric acid (12.4 mmol) prepared as in Example 3 b), in dimethoxyethane (25 ml). After 5 hours, 12.4 ml of water are added, the resulting mixture is acidified to pH=2 with concentrated HCl and is extracted with ethyl acetate. The extracts are dried and are evaporated, which leads to a syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403561B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-33b4f9404324485f9230fb6cbec40f16 |
| Source note | uspto-grants-2002_06 |