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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412958Generated: October 25, 2026

2-Bromo-1-(2,4-dimethoxyphenyl)ethanone → Methyl 4-[4-(2,4-dimethoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate

https://huagongshe.com/reaction/412958

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(2,4-dimethoxyphenyl)ethanoneHCID 98683—
ReactantMethyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylateHCID 86583815—
SolventAcetoneHCID 180—
ProductMethyl 4-[4-(2,4-dimethoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylateHCID 8675866356%

Reaction Steps

Methyl 4-[4-(2,4dDimethoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate: 99 mg (0.424 mmol) of methyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylate (Maybridge Chemical Co. LTD., Cornwall, U.K.) was dissolved in 5 mL of reagent grade acetone. 2-Bromo-2′,4′-dimethoxyacetophenone (0.440 mmol; 114 mg) was added and the solution was allowed to reflux for 2.5 h. The solution was allowed to cool and the crude product was collected as a solid and washed with methanol and dried yielding 91 mg (56% yield) of methyl 4-[4-(2,4-dimethoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562840B1
Source datasetuspto-grants-2003_05
ORD IDord-1c56195418ec450c9003b93ca63a195c
Source noteuspto-grants-2003_05