HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Z-Leu-Asp(OtBu)-Leu-OH
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-[(Phenylmethoxy)carbonyl]-L-leucine 2,5-dioxo-1-pyrrolidinyl ester | HCID 11089751 | — |
| Reactant | H-Asp(OtBu)-Leu-OH | HCID 131721134 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Z-Leu-Asp(OtBu)-Leu-OH | HCID 131721135 | 80.7% |
Reaction Steps
The H-Asp(OtBu)-Leu-OH (3.02 g), sodium bicarbonate (1.68 g), and 30 mL of water were mixed to give a mixture of pH 8. Z-Leu-OSu (3.63 g) in dioxane (30 mL) was added to the mixture and was stirred at room temp for 2 h. The reaction mixture was acidified by addition of conc. HCl to pH 1.0, then was extracted with ethyl acetate (30 mL×3). The combined extracts were dried over Na2SO4, filtered, and concentrated. The crude product was dissolved in methanol and chromatographed on a column of Sephadex™ LH20 to yield Z-Leu-Asp(OtBu)-Leu-OH as a foamy solid (4.43 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06350573B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-071582d973764280b4ea634114725c05 |
| Source note | uspto-grants-2002_02 |