HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Phthalaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | tert-Butyloxycarbonyl-phenylalanyl-leucyl-phenylalanyl-leucyl-phenylalanyl-OH | HCID 132822 | — |
| Reactant | o-Phthalaldehyde 2-mercaptoethanol | HCID 88526415 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Phthalaldehyde | HCID 4807 | — |
Reaction Steps
Four aliquots of the conjugate were hydrolyzed with concentrated HCl at 11520 C. for 20 hours and analyzed for phenylalanine. The phenylalanine was quantified as the o-phthalaldehyde/2-mercaptoethanol derivative using reverse phase HPLC with a fluorescence detector (HPLC conditions as Example 24 except the eluent gradient was 12% to 80% methanol over 20 min. and then held at 80% for 5 min.). The o-phthalaldehyde derivative was prepared as given in Example 24. For a 25 μL aliquot of the conjugate, 26 nmoles phenylalanine were found. This corresponds to 0.26 pmoles BOCPheLeuPheLeuPhe on the conjugate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06312679B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-dcc0f24a81a7464aaaa34ce3d0ffac04 |
| Source note | uspto-grants-2001_11 |