HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178516175, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | (S)-Benzyl 2-amino-3-(4-(benzyloxy)phenyl)propanoate | HCID 7408223 | — |
| Reactant | HCID 178516176 | HCID 178516176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178516175 | HCID 178516175 | — |
Reaction Steps
O-Benzyl-L-tyrosine benzyl ester (VIII) hydrochloride (0.397 g) and L-pyroglutamyl-L-histidyl-L-tryptophyl-L-serine (VII) (0.539 g) in dry dimethylformamide (50 ml) is treated with triethylamine (0.14 ml) and dicyclohexylcarbodiimide (0.227 g) in dry dimethylformamdie (5 ml) at 0° C. After stirring at room temperature for 24 hours, the reaction mixture is evaporated to dryness. The residue is triturated in methanol and the dicyclohexylurea is removed by filtration. The filtrate is concentrated to L-pyroglutamyl-L-histidyl-L-tryptophyl-L-seryl-O-benzyl-L-tyrosine benzyl ester (IX).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03953416 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-f6dcd921fdad48aaa24898bdb968449f |
| Source note | uspto-grants-1976_04 |