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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455253Generated: October 31, 2026

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

https://huagongshe.com/reaction/1455253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium peroxymonosulphateHCID 10313463—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant3-(2-methylsulfanyl-pyrimidin-4-yl)-1-oxo-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazole-2-carboxylic acid 2-chloro-benzylamideHCID 57531795—
SolventWaterHCID 962—
SolventMeOH tetrahydrofuranHCID 21899815—
Product3-(2-methanesulfonyl-pyrimidin-4-yl)-1-oxo-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazole-2-carboxylic acid 2-chloro-benzylamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482356B2
Source datasetuspto-grants-2009_01
ORD IDord-3b76ff70fa1d453f9656604b7507b82d
Source noteuspto-grants-2009_01