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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372372Generated: October 27, 2026

Tetrahydrofuran → HCID 135848671, compound

https://huagongshe.com/reaction/1372372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant2,4,6-Trichlorobenzoyl chlorideHCID 2733703—
ReactantAzilsartanHCID 135415867—
ProductHCID 135848671HCID 1358486713.3%

Reaction Steps

To a solution of 2-ethoxy-1-{[2′-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-1H-benzimidazole-7-carboxylic acid (4.0 g) and triethylamine (1.3 mL) in THF (50 mL) was added dropwise 2,4,6-trichlorobenzoyl chloride (1.4 mL) under ice-cooling. After stirring at room temperature for 12 hrs., insoluble material was filtered off and the filtrate was concentrated. The residue was dissolved in methylene chloride (50 mL) and 5-oxotetrahydro-2-furanyl (0.67 g) and N,N-dimethylaminopyridine (1.0 g) were added under ice-cooling. After stirring at room temperature for 4 hrs., the reaction mixture was diluted with chloroform (150 mL), washed with water, saturated aqueous sodium hydrogen carbonate, 1 N hydrochloric acid and saturated brine, dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography to give the title compound (0.16 g, 3.3%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157584B2
Source datasetuspto-grants-2007_01
ORD IDord-1d8be56e6b774b08bcdebdbf756793af
Source noteuspto-grants-2007_01