HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Tyrosine → HCID 131729454, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Tyrosine | HCID 6057 | — |
| Reactant | D-Alanine | HCID 71080 | — |
| Reactant | (2S)-2-amino-6-(((tert-butoxy)carbonyl)amino)hexanoic acid | HCID 2733283 | — |
| Reactant | HCID 12859615 | HCID 12859615 | — |
| Reactant | HCID 131729455 | HCID 131729455 | — |
| Reactant | HCID 131729456 | HCID 131729456 | — |
| Product | HCID 131729454 | HCID 131729454 | — |
Reaction Steps
With the exception of Z-Val-Tyr-OMe, Z-Val-Lys(Boc)-OMe and Z-Ala-Phe-D-Ala-OMe, all substrate peptides were quantitatively converted into products, i.e. the corresponding amide peptide and free carboxylic acid peptide, in 4 h reaction time. At longer reaction times also the methyl ester peptides ending with Tyr and Lys(Boc) were totally converted. Surprisingly, the methyl ester of the tripeptide with a C-terminal D-Ala residue was also converted. The HPLC analysis at 75 h reaction time showed conversion of 54 ala % of substrate to yield about 36 a/a % of the product Z-Ala-Phe-D-Ala-NH2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124372B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-572603a2517b4f6d8bb9d0640131cd1b |
| Source note | uspto-grants-2012_02 |