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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-[3-(4-fluorophenyl)-1H-pyrazol-5-yl]propyl methanesulfonate | HCID 89488474 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-fluorophenyl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole | HCID 67437281 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09314026B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-8ebacf6edac14f43937d19208f0d2d0c |
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| Source note | uspto-grants-2016_04 |
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