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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282219Generated: October 26, 2026

Methyl iodide → HCID 178503863, compound

https://huagongshe.com/reaction/1282219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-(5-Chloro-2-methyl-phenyl)-3-(1,3,5-trimethyl-1H-pyrazol-4-yl)-thioureaHCID 9857807—
SolventAcetoneHCID 180—
ProductHCID 178503863HCID 17850386374%

Reaction Steps

Under anhydrous conditions, a solution of 1-(5-Chloro-2-methyl-phenyl)-3-(1,3,5-trimethyl-1H-pyrazol-4-yl)-thiourea (2.3 g, 7.5 mmol) produced in example 8 and methyl iodide (0.94 mL, 15 mmol) in 70 mL of acetone was stirred at ambient temperature for 64 hours. The reaction mixture was concentrated in vacuo and partitioned between CH2Cl2 and saturated aqueous NaHCO3 solution. The organic phase was washed with dilute Na2S2O3 and dried (Na2SO4). Removal of solvent and crystallization of the residue from Et2O provided 1.78 g of title compound as a white solid (74% of theory, m.p. 134-135° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455566B1
Source datasetuspto-grants-2002_09
ORD IDord-5f9535551aba4e93b618843363ab3f51
Source noteuspto-grants-2002_09