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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412956Generated: October 26, 2026

Bromomethyl 4-methoxyphenyl ketone → Methyl 4-[4-(4-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate

https://huagongshe.com/reaction/412956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
ReactantMethyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylateHCID 86583815—
Reactant5-Methylthiothiophene-2-carboxylateHCID 178425923—
SolventAcetoneHCID 180—
ProductMethyl 4-[4-(4-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylateHCID 86758179104.3%

Reaction Steps

Methyl 4-]4-(4-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate: 30 mg (0.122 mmol) of methyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylate (Maybridge Chemical Co. LTD., Cornwall, U.K.) was dissolved in 1.2 mL of reagent grade acetone. 2-bromo-4′-methoxy acetophenone (0.146 mmol; 28 mg; Aldrich Chemical Co.) was added and the solution was allowed to reflux for 3 h. The solution was allowed to cool and a solid was filtered and washed with methanol and dried in vacuo to afford 46 mg (90% yield) of methyl 4-[4-(4-methoxyphenyl)(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-ca6f37ce8d1c42a9897026497f5cc565
Source noteuspto-grants-2003_05