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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212353Generated: November 2, 2026

Bromine → N-[4-[4-(4-Methoxyphenyl)-2-methyl-1,3-thiazol-5-YL]-2-pyridyl]benzamide

https://huagongshe.com/reaction/2212353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
ReactantThioacetamideHCID 2723949—
Reactant2-(2-Benzoylamino-4-pyridyl)-1-(4-methoxyphenyl)ethanoneHCID 21964260—
SolventAcetic AcidHCID 176—
ProductN-[4-[4-(4-Methoxyphenyl)-2-methyl-1,3-thiazol-5-YL]-2-pyridyl]benzamideHCID 1013569150%

Reaction Steps

Bromine (0.18 mL, 3.5 mmol) was added to a solution of 2-(2-benzoylamino-4-pyridyl)-1-(4-methoxyphenyl)ethanone (1.2 g, 3.4 mmol) in acetic acid (10 mL) and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated. The residue was dissolved in N,N-dimethylformamide (20 mL), thioacetamide (0.30 g, 19 mmol) was added to the solution and the mixture was stirred at room temperature for 20 hours. An aqueous saturated solution of sodium hydrogencarbonate (20 mL) was added to the reaction mixture, the resulting mixture was extracted with ethyl acetate and the extract was washed with water. The extract was dried and concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate, 1:1) to obtain 0.68 g (yield 50%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101899B1
Source datasetuspto-grants-2006_09
ORD IDord-7f361e30365f42a1b6b7e91bdbb1d651
Source noteuspto-grants-2006_09