HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Leucinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-benzoyl-L-alanine | HCID 709778 | — |
| Reactant | Bz-Ala-Leu-NH2 | HCID 131712768 | — |
| Reactant | Bz-Ala-Leu-OH | HCID 131712769 | — |
| Solvent | Potassium Chloride | HCID 4873 | — |
| Product | Leucinamide | HCID 69640 | — |
| Product | Bz-Ala-Leu-NH2 | HCID 131712768 | — |
Reaction Steps
To a solution of 2 ml 15 mM Bz-Ala-Leu-NH2 in 0.1 M KCl-1 mM EDTA, pH 9.7, 25° C. and 10% dimethyl formamide was added 2 mg CPD-Y. The reaction course as shown on FIG. 5 was followed by HPLC as described in example 1. It is seen that Bz-Ala-Leu-NH2 after 20 minutes was completely converted to about 68% Bz-Ala-Leu-OH and 32% Bz-Ala-OH. Amino acid analysis on the reaction mixture showed that the Bz-Ala-OH was mainly formed by cleavage of Leu-NH2 from Bz-Ala-Leu-NH2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04339534 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-3e4e57be78a54b6da6fc67e0116d6d94 |
| Source note | uspto-grants-1982_07 |