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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837953Generated: November 2, 2026

Water → 5-(2-Thienyl)-2-dimethylaminopyridine

https://huagongshe.com/reaction/1837953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-BromothiopheneHCID 13851—
Reactant5-bromo-N,N-dimethylpyridin-2-amineHCID 3803041—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product5-(2-Thienyl)-2-dimethylaminopyridineHCID 2267766129.5%

Reaction Steps

To a suspension of magnesium (0.119 g, 4.97 mmol) in THF (3 mL) was added 2-bromothiophene (0.811 g, 4.97 mmol) and the reaction mixture was stirred for 3 h. Another equivalent of 2-bromothiophene (0.811 g, 4.97 mmol) was added and the reaction mixture was heated at the reflux temperature for 2 h, then allowed to cool to room temperature. The resulting mixture was added to a solution of 5-bromo-2-dimethylaminopyridine (1.0 g, 4.97 mmol) in THF (12 mL) and the reaction was heated at the reflux temperature for 11 h, then was allowed to cool to room temperature. The resulting mixture was treated with water (10 mL), extracted with EtOAc (3×30 mL), dried (MgSO4) and concentrated under reduced pressure. The crude product was purified by flash chromatography (10% EtOAc/hex) to give 5-(2-thienyl)-2-dimethylaminopyridine (0.3 g, 29%): TLC (10% EtOAc/hex) Rf 0.24; HPLC ES-MS m/z (relative abundance) 205 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784167B2
Source datasetuspto-grants-2004_08
ORD IDord-4d2b9cdea0ab4f9d94dc5b9b63f2b98b
Source noteuspto-grants-2004_08