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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337524Generated: October 25, 2026

Triethylamine → 2-Amino-4-(2-pyridyl)thiazol-5-yl 2-pyridyl ketone

https://huagongshe.com/reaction/337524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
ReactantThioureaHCID 2723790—
Reactant1,3-Di(2-pyridyl)-1,3-propanedioneHCID 2728494—
SolventAcetic AcidHCID 176—
Product2-Amino-4-(2-pyridyl)thiazol-5-yl 2-pyridyl ketoneHCID 2314466851%

Reaction Conditions

Temperature80 °C

Reaction Steps

1,3-Di(2-pyridyl)propane-1,3-dione (1.17 g, 5.15 mmol) was dissolved in acetic acid (20 mL), and bromine (856 mg, 5.35 mmol) was added thereto, followed by stirring at 80° C. for 1 hour. The reaction mixture was concentrated under reduced pressure, and the resulting residue was suspended in ethanol (30 mL), and triethylamine (0.750 mL, 5.38 mmol) and thiourea (416 mg, 5.47 mmol) were added thereto, followed by stirring under heating and reflux for 30 minutes. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction mixture, followed by extraction with chloroform. The solvent was distilled away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (chloroform:methanol=9:1) to afford the entitled Compound 630 (739 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889718B2
Source datasetuspto-grants-2014_11
ORD IDord-7e627cebae7242b3b99a599af6b579b3
Source noteuspto-grants-2014_11