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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751280Generated: October 30, 2026

Sodium Iodide → 5-Iodopyrazolo[1,5-A]pyrimidine

https://huagongshe.com/reaction/751280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetyl chlorideHCID 6367—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium SulfiteHCID 24437—
Reactant5-Chloropyrazolo(1,5-a)pyrimidineHCID 21071759—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Product5-Iodopyrazolo[1,5-A]pyrimidineHCID 4976153151.7%

Reaction Steps

Dissolve 5-chloro-pyrazolo[1,5-a]pyrimidine (Hans Reimlinger et al., Chem. Ber. 1970, 103, 3252-3265; 1.15 g, 7.5 mmol) and sodium iodide (5.6-g, 37.4 mmol) in anhydrous acetonitrile (50 mL). Add acetyl chloride (2.7 ml, 37.9 mmol). Stir and reflux under nitrogen for 20 h. Pour the reaction mixture into a stirring mixture of 0.5M aqueous potassium carbonate (200 mL), 1.0M aqueous sodium sulfite (50 mL), and diethyl ether (350 mL). Separate the organic layer, dry over anhydrous magnesium sulfate, filter and concentrate under reduced pressure. Chromatograph the crude product on flash silica using neat dichloromethane to obtain 950 mg (51%) of the title compound as a yellow solid. TOF MS ES+ exact mass calculated for C6H4N310): m/z=245.9528; Found: 245.9517. 1H NMR (400 MHz, DMSO-d6) δ 8.82 (d, J=7 Hz, 1H), 8.18 (d, J=2 Hz, 1H), 7.32 (d, J=7 Hz, 1H), 6.69 (d, J=2 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405299B2
Source datasetuspto-grants-2008_07
ORD IDord-7d5e51ceb5694f19a478045568068a57
Source noteuspto-grants-2008_07