HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tosyl-L-asparagine → (2S)-6-[[(2S)-4-amino-4-oxo-2-(p-tolylsulfonylamino)butanoyl]amino]-2-[(4-aminophenyl)sulfonyl-isobutyl-amino]hexanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tosyl-L-asparagine | HCID 6995570 | — |
| Reactant | Nalpha-isobutyl-Nalpha-(4-nitrobenzenesulfonyl)-L-lysine hydrochloride | HCID 69107784 | — |
| Product | (2S)-6-[[(2S)-4-amino-4-oxo-2-(p-tolylsulfonylamino)butanoyl]amino]-2-[(4-aminophenyl)sulfonyl-isobutyl-amino]hexanoic acid | HCID 508570 | — |
Reaction Steps
The title compound was prepared from Nα-isobutyl-Nα-(4-nitrobenzenesulfonyl)-L-lysine hydrochloride (400 mg, 1.03 mmol, example 5, step C) as described in general procedure Bc using Nα-(4-methylbenzenesulfonyl)-L-asparagine (286 mg, 1.0 mmol) which was prepared in step A this example. The final product, Nα-isobutyl-Nα-(4-nitrobenzenesulfonyl)-Nε-[N′α-(4-methylbenzenesulfonyl)-L-asparagyl]-L-lysine was subsequently hydrogenolysed following the indications of general procedure E. Purification by HPLC gave the desired material (185 mg, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06656965B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-52833547ee0541e0b351b535480815b3 |
| Source note | uspto-grants-2003_12 |