HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → (R)-4'-Methyl-N-(1-(6-methylpyridin-3-yl)ethyl)-5-(pyrimidin-2-yloxy)biphenyl-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| 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 | 4'-Methyl-5-(pyrimidin-2-yloxy)biphenyl-3-carboxylic acid | HCID 58188034 | — |
| Reactant | (R)-1-(6-Methylpyridin-3-yl)ethan-1-amine dihydrochloride | HCID 67053782 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-4'-Methyl-N-(1-(6-methylpyridin-3-yl)ethyl)-5-(pyrimidin-2-yloxy)biphenyl-3-carboxamide | HCID 58188241 | — |
Reaction Steps
To a solution of 4′-methyl-5-(pyrimidin-2-yloxy)biphenyl-3-carboxylic acid (20 mg, 0.065 mmol) in N,N-dimethylformamide (1 mL) were added (R)-1-(6-methylpyridin-3-yl)ethanamine dihydrochloride (30 mg, 0.143 mmol), N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (60 mg, 0.16 mmol), and N,N-diisopropylethylamine (200 μL, 1.15 mmol). The reaction mixture was stirred at room temperature for 16 hours. LC-MS indicated the reaction was complete. The reaction mixture was purified by preparative HPLC (100×21.2 mm C18 column, CH3CN/water[10 mM Et2NH]) to afford a light color solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946439B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-30489d44cbcd411fa2b3641306d29216 |
| Source note | uspto-grants-2015_02 |