HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Glutamine → Boc-L-Valine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Glutamine | HCID 5961 | — |
| Reactant | L-Threonine | HCID 6288 | — |
| Reactant | L-Tryptophan | HCID 6305 | — |
| Reactant | L-Isoleucine | HCID 6306 | — |
| Reactant | 1,2-Ethanedithiol | HCID 10902 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Product | Boc-L-Valine | HCID 83693 | — |
Reaction Steps
A larger excess of 6 to 8 equivalents is used in the coupling of steps (h) and (m) with the tert-butoxycarbonyl-protected amino acids aparagine, glutamine, isoleucine, proline, and threonine. In the cycles following addition of a tryptophane residue, 2% 1,2-ethanedithiol (FLUKA) is added to the deprotection steps (a) and (b) in order to prevent the oxidation of the indole ring. Dehydration of the carboxamide function of glutamine is minimized by preforming the 1-hydroxybenzotriazole ester (0°, 15 min) before addition to the resin in step (h).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05656596 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-c03513d166bf4d9d933f5a2eda0b8657 |
| Source note | uspto-grants-1997_08 |