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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078345Generated: November 2, 2026

Hydrochloric Acid → 3-[3-(N-benzyl-N-methylamino)-propyloxy]-2-methyl-5-(2-fluorophenyl)-pyrazole

https://huagongshe.com/reaction/1078345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-benzyl-3-chloro-N-methylpropan-1-amineHCID 22067—
ReactantSodium hydrideHCID 24758—
Reactant2-Methyl-5-(2-fluorophenyl)-pyrazolin-3-oneHCID 22902355—
SolventAcetoneHCID 180—
SolventIsopropanolHCID 3776—
Solventtert-Butyl methyl etherHCID 15413—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Product3-[3-(N-benzyl-N-methylamino)-propyloxy]-2-methyl-5-(2-fluorophenyl)-pyrazoleHCID 2290238974.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

3.3 g of 2-methyl-5-(2-fluorophenyl)-pyrazolin-3-one were dissolved in 50 ml of 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidone. 0.55 g of sodium hydride (as an 80% strength solution in paraffin) was added to this solution and the reaction mixture was stirred at 80° C. for 30 minutes. 3.3 g of 3-(N-benzyl-N-methylamino)-propyl chloride were added to the reaction mixture which was stirred at 80° C. for a further 2 hours. After the reaction mixture had cooled, 10 ml of a 2N solution of hydrochloric acid in isopropanol were added to it, and the mixture was then added dropwise to 2 liters of a 1:3 mixture of acetone and tert-butyl methyl ether. The resulting precipitate was filtered out and dissolved in a mixture of saturated aqueous sodium carbonate solution and ethyl acetate. The organic phase was separated and the aqueous phase was subsequently extracted repeatedly with ethyl acetate. The combined ethyl acetate extracts were dried with sodium sulfate and evaporated. The crude base obtained was purified by chromatography on silica gel. 4.4 g of 3-[3-(N-benzyl-N-methylamino)-propyloxy]-2-methyl-5-(2-fluorophenyl)-pyrazole were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05547967
Source datasetuspto-grants-1996_08
ORD IDord-4ea41e00dfa647b7ad51b907bd34a741
Source noteuspto-grants-1996_08