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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851408Generated: November 1, 2026

2-Bromothiazole → Benzyl 2-amino-3-(1,3-thiazol-2-ylethynyl)benzoate

https://huagongshe.com/reaction/1851408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromothiazoleHCID 76430—
ReactantBenzyl 2-amino-3-ethynylbenzoateHCID 57901749—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 2-amino-3-(1,3-thiazol-2-ylethynyl)benzoateHCID 5790168682%

Reaction Steps

A solution of benzyl 2-amino-3-ethynylbenzoate (3.06 g), 2-bromothiazole (1.65 mL), bis(triphenylphosphine)palladium(II) dichloride (0.704 g) and copper iodide (0.232 g) in triethylamine (60 mL) was stirred under a nitrogen atmosphere at 60° C. for 1.5 hr with heating. The reaction mixture was diluted with ethyl acetate and filtered through celite. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=10:90-50:50) to give the title compound (3.32 g, yield 82%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-630f7093ad7b485996d9b57e4524f054
Source noteuspto-grants-2015_02