Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500711Generated: October 26, 2026

Isopropyl iodide → 4-(3-iodo-1-isopropyl-1H-pyrazol-4-yl)-2-(methylthio)pyrimidine

https://huagongshe.com/reaction/500711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantHexaneHCID 8058—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(5-Iodo-1H-pyrazol-4-yl)-2-(methylsulfanyl)pyrimidineHCID 46864160—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(3-iodo-1-isopropyl-1H-pyrazol-4-yl)-2-(methylthio)pyrimidineHCID 5942440947.2%

Reaction Steps

A mixture of 4-(5-iodo-1H-pyrazol-4-yl)-2-(methylthio)pyrimidine (A) (31.8 g, 0.1 mol), 2-iodo-propane (85 g, 50 mL, 0.5 mol) and K2CO3 (16.5 g, 0.12 mol) in DMF (500 mL) was heated at 40˜50° C. overnight. When TLC (hexane: EtOAc=15:1) showed the reaction was complete, DMF was evaporated under reduced pressure. The residue was taken up with EtOAc (400 mL). The mixture was washed with saturated aqueous NaCl, dried over Na2SO4 and concentrated to give crude product, which was purified via prep. HPLC to give pure 4-(3-iodo-1-isopropyl-1H-pyrazol-4-yl)-2-(methylthio)pyrimidine B-1-1 (17 g, 47.2%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772246B2
Source datasetuspto-grants-2010_08
ORD IDord-78b3fc8fdc9c418a8074fbf09cc9a9a1
Source noteuspto-grants-2010_08