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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380289Generated: October 31, 2026

Methyl iodide → 4-Methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/2380289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant4H,5H,6H,7H-pyrazolo(1,5-a)pyrimidineHCID 135627629—
SolventDimethylformamideHCID 6228—
Product4-Methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidineHCID 15077743—

Reaction Steps

To a suspension of 62% sodium hydride (1.41 g) in N,N-dimethylformamide (30 ml) was added 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine (4.5 g) under ice-cooling. To this solution was added dropwise methyl iodide (2.27 ml) under ice-cooling, and the mixture was stirred at the same temperature for 1.5 hours. The reaction mixture was poured into ethyl acetate (50 ml), and the resulting precipitate was filtered off. The filtrate was evaporated to give 4-methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine (5.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05366970
Source datasetuspto-grants-1994_11
ORD IDord-27438b75cbf948a0ae7430f12ffc8ab0
Source noteuspto-grants-1994_11