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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(2-Isopropyl-pyrazolo[1,5-a]pyridin-3-yl)-2-methyl-propan-1-ol | HCID 13391703 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Isopropyl-3-(1-methoxy-2-methylpropyl)pyrazolo[1,5-a]pyridine | HCID 20242526 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04578392 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-6a97749c826a467c8a324751dd461b9d |
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| Source note | uspto-grants-1986_03 |
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