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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065049Generated: October 29, 2026

Bromide ion → HCID 66928948, compound

https://huagongshe.com/reaction/2065049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantNitrogenHCID 947—
ReactantPotassium CarbonateHCID 11430—
Reactant4-nitro-1H-pyrazoleHCID 16376—
Reactant(5-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-2-yl)methyl methanesulfonateHCID 86649489—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 66928948HCID 66928948—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of methanesulfonic acid 5-(2-methyl-[1,3]dioxolan-2-yl)-thiazol-2-ylmethyl ester (520 mg, 1.86 mmol) in acetone (15.0 mL) was added to a solution of 4-nitro-1H-pyrazole (221 mg, 1.96 mmol) in acetone (15.0 mL). K2CO3 (1.300 g, 9.31 mmol) followed by TBA bromide (120 mg, 0.37 mmol) were added and the reaction mixture was stirred at rt overnight. Water (10 mL) and EA (10 mL) were added. The aq. layer was extracted with EA (10 mL) and the combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (10:1 to 2:1 hept-EA) gave the title compound as a yellow oil. TLC: rf (1:2 hept-EA)=0.15. LC-MS-conditions 01: tR=0.83 min, [M+H]+=296.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-79a18a2ae8b04375ae926d64d2cca31b
Source noteuspto-grants-2012_10