HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 3-(2-methanesulfonyl-pyrimidin-4-yl)-1-oxo-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazole-2-carboxylic acid 2-chloro-benzylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 3-(2-methylsulfanyl-pyrimidin-4-yl)-1-oxo-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazole-2-carboxylic acid 2-chloro-benzylamide | HCID 57531795 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 3-(2-methanesulfonyl-pyrimidin-4-yl)-1-oxo-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazole-2-carboxylic acid 2-chloro-benzylamide | HCID 57531792 | — |
Reaction Steps
To a solution of 3-(2-methylsulfanyl-pyrimidin-4-yl)-1-oxo-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazole-2-carboxylic acid 2-chloro-benzylamide, 15, (0.20 g, 0.48 mmol) in THF/MeOH (8 mL of 1:1 mixture) was added dropwise a solution of Oxone® (potassium peroxymonosulfate) (in H2O (8 mL). After stirring the reaction for 1.5 h at room temperature, the solution was poured into aqueous saturated NaHCO3. The aqueous phase is extracted with CHCl3 (×3). The combined organic phases are dried (MgSO4), filtered and concentrated in vacuo to afford the desired product which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07482356B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-3b76ff70fa1d453f9656604b7507b82d |
| Source note | uspto-grants-2009_01 |