HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-[N-[(3S)-3-Amino-2-hydroxybutyl]-L-phenylalanvl]-L-leucine, dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-[(3S)-3-[[(t-Butyloxy)carbonyl]amino]-2-hydroxybutyl]-L-phenylalanyl-L-leucine, t-butyl ester | HCID 13933328 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-[N-[(3S)-3-Amino-2-hydroxybutyl]-L-phenylalanvl]-L-leucine, dihydrochloride | HCID 131714412 | — |
Reaction Steps
A solution of N-[N-[(3S)-3-[[(t-butyloxy)carbonyl]amino]-2-hydroxybutyl]-L-phenylalanyl-L-leucine, t-butyl ester (slower isomer) (0.27 g, 0.52 mmol) in 20 ml of 1.3N hydrogen chloride in acetic acid was allowed to stir for 2 hours at room temperature, during which time a white precipitate separated. The mixture was concentrated under reduced pressure to approximately one third of the original volume, then diluted with ether and filtered yielding 185 mg of the title compound as a white solid, melting point 236°-239° C. (with slow decomposition >210° C.). Analysis by 400 MHz 1H-NMR revealed the presence of a small amount (<5%) of the faster isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670541 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-b2b21e3aab68406a8320626290a49c86 |
| Source note | uspto-grants-1987_06 |