HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 131711694, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl (S)-(2-((2,5-dioxo-1-pyrrolidinyl)oxy)-1-(1H-indol-3-ylmethyl)-2-oxoethyl)carbamate | HCID 98767 | — |
| Reactant | HCID 131711695 | HCID 131711695 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131711694 | HCID 131711694 | 65.3% |
Reaction Steps
2.2 g (5.3 mmoles) of H-Leu-Asp-L-Phg-NH2.HCl, prepared as described in Example 6, Step 3, are reacted with 2.32 g (5.8 mmoles) of BOC-Trp-OSu in 50 ml of DMF in the presence of 1.48 ml (10.6 mmoles) of triethylamine. Next day the reaction mixture is evaporated in vacuo and the residue is triturated with water. The obtained crude product, weighing 3.30 g, is crystallized from 70 ml of 80% ethanol under decolourizing. 2.30 g (65%) of BOC-Trp-Leu-Asp-L-Phg-NH2 are obtained; m.p.: 205°-207° C. (decomposition), Rf5 : 0.40, [α]D : -7.3° (c: 1.0, in dimethyl formamide).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04183909 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-50a81e9881214f4ab0388e49fed11b64 |
| Source note | uspto-grants-1980_01 |