HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nalpha-isobutyl-Nalpha-(4-nitrobenzenesulfonyl)-L-lysine hydrochloride → (2S)-2-[(4-aminophenyl)sulfonyl-isobutyl-amino]-6-[[(2S)-2-[[2-(4-methoxyphenyl)acetyl]amino]-3-phenyl-propanoyl]amino]hexanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nalpha-isobutyl-Nalpha-(4-nitrobenzenesulfonyl)-L-lysine hydrochloride | HCID 69107784 | — |
| Reactant | Nalpha-(4-methoxyphenylacetyl)-L-phenylalanine | HCID 69347446 | — |
| Product | (2S)-2-[(4-aminophenyl)sulfonyl-isobutyl-amino]-6-[[(2S)-2-[[2-(4-methoxyphenyl)acetyl]amino]-3-phenyl-propanoyl]amino]hexanoic acid | HCID 508685 | — |
Reaction Steps
The title compound was prepared from Nα-isobutyl-Nα-(4-nitrobenzenesulfonyl)-L-lysine hydrochloride (200 mg, 0.45 mmol, example 5, step C) as described in general procedure Bc using Nα-(4-methoxyphenylacetyl)-L-phenylalanine (example 132, step A). The final product, Nα-isobutyl-Nα-(4-nitrobenzenesulfonyl)-Nε-[N′α-(4-methoxyphenylacetyl)-L-phenylalanyl]-L-lysine was subsequently hydrogenolysed following the indications of general procedure E. Purification by HPLC gave the desired material (7 mg, 4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608100B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-4d0850293d684c58a3e6d91058252d53 |
| Source note | uspto-grants-2003_08 |