HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Methyl 3-((3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)carbamoyl)benzyl)thio)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-amino-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide | HCID 66587027 | — |
| Reactant | Methyl 3-(3-(chlorocarbonyl)benzylthio)propanoate | HCID 86705202 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-((3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)carbamoyl)benzyl)thio)propanoate | HCID 66587735 | — |
Reaction Steps
To a solution of 2-amino-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide (138 mg, 0.37 mmol, 1.00 equiv) in tetrahydrofuran (6 mL) was added methyl 3-(3-(chlorocarbonyl)benzylthio)propanoate (112 mg, 0.41 mmol, 1.10 equiv) and pyridine (60 mg, 0.76 mmol, 2.00 equiv) and the resulting solution was stirred for 5 h at room temperature. The reaction progress was monitored by LCMS. The crude product was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809339B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-66280a5bcbb64bd49dc8232011e20201 |
| Source note | uspto-grants-2014_08 |