HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 131722627, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10070574 | HCID 10070574 | — |
| Reactant | HCID 131722628 | HCID 131722628 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131722627 | HCID 131722627 | — |
Reaction Steps
The title compound was obtained by analogous manner as described in Example 18, but using BocTyr(PO3Et2)OH. The N-acetylation was performed by treatment of crude H—Tyr(PO3Et2)—Val—Asn—Val—NH2 with 1.5 equiv. of DIEA and 5 equiv. of acetic anhydride in DMF for 2 h at 25° C. The final compound was obtained with chromatographic purity (HPLC) of 90.0%. Amino acid ratios: Val 2 (2); Asx 1.17 (1); Tyr 0.87 (1). Peptide content: 83%. FAB mass spectroscopy; m/z 671 [M—H]+. (MW 670.1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06245742B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-5353513a0c4f42509da40dcf791777d5 |
| Source note | uspto-grants-2001_06 |