HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-(3-(chloromethyl)benzamido)-N-(5-phenylpyrimidin-2-yl)-5-(piperidin-1-yl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(Chloromethyl)benzoyl chloride | HCID 2733324 | — |
| Reactant | 2-amino-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide | HCID 66587027 | — |
| Solvent | Tetrahydrofurane dichloromethane | HCID 21919333 | — |
| Product | 2-(3-(chloromethyl)benzamido)-N-(5-phenylpyrimidin-2-yl)-5-(piperidin-1-yl)benzamide | HCID 66588180 | — |
Reaction Steps
To a 0° C. solution of 100 mg of 2-amino-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide 2d, and 138 mg of diisopropylethylamine in 2 mL of 1:1 THF/DCM was added dropwise 46 mg of 3-(chloromethyl)benzoyl chloride. The mixture was stirred overnight at room temperature and the solvent was evaporated. All of this material was used in the next step without further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09289429B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-9b7af72ccab74b4f9d28511fb077dff7 |
| Source note | uspto-grants-2016_03 |