HuagongsheHuagongshe Chemistry Print Report · For research reference only
benzyl (2S)-2-aminopropanoate → HCID 178447405, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | benzyl (2S)-2-aminopropanoate | HCID 726858 | — |
| Reactant | HCID 178447599 | HCID 178447599 | — |
| Reactant | HCID 178500357 | HCID 178500357 | — |
| Reactant | HCID 178500358 | HCID 178500358 | — |
| Reactant | HCID 178512944 | HCID 178512944 | — |
| Product | HCID 178447405 | HCID 178447405 | — |
Reaction Steps
By substituting nitro-L-arginine benzyl ester for the L-alanine benzyl ester in the procedure of Example 23, and then treating the product by the procedures of Examples 24 and 26, Nα -(4-methoxycarbonyl-2-methylbutanoyl)-nitro-L-arginine benzyl ester, Nα -(4-methoxycarbonyl-2-methylbutanoyl)-L-arginine, and Nα -(4-carboxy-2-methylbutanoyl)-L-arginine are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04105789 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-3c1d709c85fd43cdb6ef54bba328f3e5 |
| Source note | uspto-grants-1978_08 |