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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081080Generated: October 25, 2026

Cesium carbonate → HCID 24810137, compound

https://huagongshe.com/reaction/2081080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant3-Bromomethyl-4-chloro-thieno[3,2-c]pyridine-7-carboxylic acid ethyl esterHCID 11530097—
Reactant2-methyl-5-(1-methyl-1H-[1,2,3]triazol-4-yl)-phenolHCID 59649710—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 24810137HCID 24810137—

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of cesium carbonate (0.56 g, 1.73 mmol) (Aldrich), 2-methyl-5-(1-methyl-1H-[1,2,3]triazol-4-yl)-phenol (0.24 g, 1.27 mmol) (from Example 21 supra) in tetrahydrofuran-N,N-dimethylformamide (5:2, 17.5 mL) was heated at 70° C. for 3 hours. 3-Bromomethyl-4-chloro-thieno[3,2-c]pyridine-7-carboxylic acid ethyl ester (0.40 g, 1.15 mmol) (from Example 1 supra) was added. Heating was continued for 18 hours. The reaction mixture was partitioned between ethyl acetate and water. The aqueous phase was extracted with ethyl acetate (2×). The combined organic phase washed with water and brine, dried (MgSO4) and concentrated. The residue was purified by flash chromatography eluting with 30% ethyl acetate in dichloromethane to give 4-chloro-3-[2-methyl-5-(1-methyl-1H-[1,2,3]triazol-4-yl)-phenoxy-methyl]-thieno[3,2-c]pyridine-7-carboxylic acid ethyl ester. (Yield 0.25 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932390B2
Source datasetuspto-grants-2011_04
ORD IDord-a19d972dec2649108b9a87de5024a04d
Source noteuspto-grants-2011_04