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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628461Generated: October 28, 2026

Sodium Iodide → 2-(4-fluorophenyl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole

https://huagongshe.com/reaction/628461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-[3-(4-fluorophenyl)-1H-pyrazol-5-yl]propyl methanesulfonateHCID 89488474—
SolventDimethylformamideHCID 6228—
Product2-(4-fluorophenyl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazoleHCID 67437281—

Reaction Conditions

Temperature10 °C

Reaction Steps

To a solution of crude 3-[3-(4-fluorophenyl)-1H-pyrazol-5-yl]propyl methanesulfonate (52 g, 0.122 mol), in 300 mL N,N′-Dimethylformamide is added at 10° C. sodium iodide (1.84 g, 12.2 mmol). Then, sodium hydride (60%, 5.4 g, 0.134 mol) is added portionwise and the mixture is stirred for 30 min at 10° C. followed by 1 h at room temperature. To the resulting brown suspension is added saturated ammonium chloride and the mixture is extracted with ethyl acetate. The extracts are dried and evaporated in vacuo. The obtained crude product is purified by trituration with 50 mL water+50 mL n-hexane. After drying of the solid in vacuo 22.9 g (90%) of the product is obtained and is being used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09314026B2
Source datasetuspto-grants-2016_04
ORD IDord-8ebacf6edac14f43937d19208f0d2d0c
Source noteuspto-grants-2016_04