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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661064Generated: October 30, 2026

Methanol → 5-(5-(3-chloropropylthio)-4-methyl-4H-1,2,4-triazol-3-yl)-2,4-dimethylthiazole

https://huagongshe.com/reaction/1661064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178432727HCID 178432727—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product5-(5-(3-chloropropylthio)-4-methyl-4H-1,2,4-triazol-3-yl)-2,4-dimethylthiazoleHCID 4462789837.5%

Reaction Conditions

Temperature22 °C

Reaction Steps

5-(2,4-dimethylthiazol-5-yl)-4-methyl-4H-1,2,4-triazole-3-thiol (Prep27, 5 g, 22 mmol) was added to a mixture of methanol (15 ml) and acetone (35 ml), followed by K2CO3 (5 g, 36 mmol) and 1-bromo-3-chloropropane (35 ml, 36 mmol). The suspension was stirred at 22° C. for 24 h. The volume of solvent was reduced, then ethyl acetate (63 ml) was added and the organic layer was washed with water, the EA was removed under vacuum and the crude purified by FC (EA/MeOH 15:1) to afford 2.5 g of pure product (y=37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030322B2
Source datasetuspto-grants-2011_10
ORD IDord-10eff361006c4b3ea2b609b2d6ddd6a3
Source noteuspto-grants-2011_10