HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178462102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | (S)-2-{[(R)-5-(4-bromo-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carbonyl]-amino}-propionic acid | HCID 58431145 | — |
| Reactant | HCID 178420791 | HCID 178420791 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178462102 | HCID 178462102 | 16.2% |
Reaction Steps
To a cold (0° C.) solution of (S)-2-{[(R)-5-(4-bromo-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carbonyl]-amino}-propionic acid (0.050 g, 0.088 mmol) in DMF (1 mL) was added (R)-3-(1H-tetrazol-5-yl)-piperidine trifluoro-acetic acid salt (0.047 g, 0.18 mmol), HATU (0.040 g, 0.11 mmol) and Et3N (0.026 mL, 0.18 mmol). The reaction was allowed to stir for 10 minutes and HOAt (0.024 g, 0.18 mmol) was added and the mixture allowed to warm to room temperature overnight. The crude reaction mixture was purified by reverse-phase HPLC to give 10 mg of the title compound as a white solid, m/z 701.4 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552205B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-6a9e394a8ad94e1ebf40d8fa288c8319 |
| Source note | uspto-grants-2013_10 |