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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483088Generated: October 27, 2026

Methyl iodide → 2-Isopropyl-3-(1-methoxy-2-methylpropyl)pyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/483088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(2-Isopropyl-pyrazolo[1,5-a]pyridin-3-yl)-2-methyl-propan-1-olHCID 13391703—
SolventTetrahydrofuranHCID 8028—
Product2-Isopropyl-3-(1-methoxy-2-methylpropyl)pyrazolo[1,5-a]pyridineHCID 2024252688%

Reaction Steps

To a suspension of 1.24 g of sodium hydride (55% oil suspension) in 20 ml of tetrahydrofuran was slowly added a solution of 3 g of 2-isopropyl-3-(1-hydroxy-2-methylpropyl)pyrazolo[1,5-a]pyridine in 5 ml of dry tetrahydrofuran under stirring and cooling. After the addition was completed, the stirring was continued for 5 minutes at room temperature, then reflux temperature for 15 minutes. The mixture was cooled with ice-water, to which 5.5 g of methyl iodide were added, and stirred for an hour at room temperature. After treating with aqueous 20% ammonium chloride solution, the mixture was extracted with ether. The ether layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to dryness. The residue was applied to silica gel column chromatography, eluted with ethyl acetate-benzene (1:4) to give 2.8 g (88%) of the desired product as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04578392
Source datasetuspto-grants-1986_03
ORD IDord-6a97749c826a467c8a324751dd461b9d
Source noteuspto-grants-1986_03