HuagongsheHuagongshe Chemistry Print Report · For research reference only
Leucinamide → N-(tert-Butoxycarbonyl)-L-phenylalanyl-L-leucinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Leucinamide | HCID 69640 | — |
| Reactant | L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]- | HCID 77857 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-(tert-Butoxycarbonyl)-L-phenylalanyl-L-leucinamide | HCID 15030956 | — |
Reaction Steps
1 ml 0.1M veronal-Na/HCl buffer, pH 8.3/50% (v/v) DMSO, containing 100 mM Boc-Phe-OCam, 300 mM H-Leu-NH2 and 100 μM trypsinogen is agitated at room temperature under pH control. After 3 hours, the reaction is stopped as described in Example 3. The yield is analytically determined with HPLC to be 93% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05369018 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-8c0a42b33beb437d98f0b9d43cf70277 |
| Source note | uspto-grants-1994_11 |