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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186605Generated: October 29, 2026

2-Bromo-1-(4-chloropyridin-3-yl)ethan-1-one → Methyl 4-[4-(4-chloro(3-pyridyl))(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate

https://huagongshe.com/reaction/2186605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(4-chloropyridin-3-yl)ethan-1-oneHCID 18537456—
ReactantMethyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylateHCID 86583815—
Reactant5-Methylthiothiophene-2-carboxylateHCID 178425923—
ProductMethyl 4-[4-(4-chloro(3-pyridyl))(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylateHCID 8675818080.4%

Reaction Steps

Methyl 4-4-(4-chloro(3-pyridyl))(3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate: 240 mg (0.970 mmol) of methyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylate (Maybridge Chemical Co. LTD., Cornwall, U.K.) was reacted with 2-bromo-1-(4-chloro(3-pyridyl))ethan-1-one (1.06 mmol; 250 mg) in a manner similar to Example 22, step (a) to afford 286 mg (77% yield) of methyl 4-[4-(4-chloro(3-pyridyl))(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403633B2
Source datasetuspto-grants-2002_06
ORD IDord-74684349609842b6b455d4a2bd75d9e9
Source noteuspto-grants-2002_06