HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178476757, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| 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 | Ethyl 3-((R)-amino(phenyl)methyl)phenyl(methyl)phosphinate | HCID 89462476 | — |
| Reactant | HCID 178524762 | HCID 178524762 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178476757 | HCID 178476757 | — |
Reaction Steps
To a stirred solution of 4-hydroxy-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxylic acid, 8-b, (7.9 g, 25.7 mmol) and Et3N (7.09 g, 70.2 mmol) in MeCN (50 ml) was added HATU (10.7 g, 28.2 mmol). The mixture was stirred for 10 min at room temperature and then ethyl 3-((R)-amino(phenyl)methyl)phenyl(methyl)phosphinate, 24-e, (6.79 g, 23.4 mmol) was added. The resulting mixture was stirred at room temperature for 1 hour. The mixture was then concentrated under vacuum and the residue was taken into ethyl acetate followed by washing with saturated NH4Cl. The organic layer was dried over sodium sulfate and concentrated under vacuum to provide the crude product, 24-f, (18.8 g) as red oil. The crude product was used for the next step directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09079930B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-722713215bca498dbc547498ab7b7384 |
| Source note | uspto-grants-2015_07 |