HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(1-(4-(pyridin-2-yl)pyrimidin-2-yl)piperidin-4-yl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Chloro-4-(pyridin-2-yl)pyrimidine | HCID 16122291 | — |
| Reactant | N-(Piperidin-4-yl)methanesulfonamide | HCID 16227261 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(1-(4-(pyridin-2-yl)pyrimidin-2-yl)piperidin-4-yl)methanesulfonamide | HCID 67508213 | 78% |
Reaction Steps
A solution of 2-chloro-4-(pyridin-2-yl)pyrimidine (0.576 g, 3 mmol), N-(piperidin-4-yl)methanesulfonamide (0.64 g, 3.6 mmol) and Et3N (0.77 mL, 6 mmol) in CH3CN (15 mL) was refluxed for 2 h and TLC (petroleum:EtOAc=5:1) showed the reaction was complete. The reaction mixture was concentrated and purified by chromatography, eluted with CH2Cl2:MeOH (10:1 to 5:1) to give the title compound (0.78 g, 78%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056865B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-7662f2ac1bae4eda877f713096552496 |
| Source note | uspto-grants-2015_06 |