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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874517Generated: November 1, 2026

Triethylamine → HCID 57749236, compound

https://huagongshe.com/reaction/1874517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantHCID 57749262HCID 57749262—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57749236HCID 5774923679%

Reaction Steps

To a solution of methyl 3-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]benzoate (4.20 g, 13.9 mmol) and triethylamine (3.47 μL, 25.1 mmol) in tetrahydrofuran (40 mL) was added with stirring under ice-cooling cyclopropanecarbonyl chloride (1.52 mL, 16.7 mmol), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was dissolved in ethanol (50 mL). 8N Aqueous sodium hydroxide solution (7 mL) was added thereto, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was adjusted to pH 4 with 6N hydrochloric acid, and the precipitated solid was collected by filtration and washed with water to give the title compound (3.90 g, 79%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-0a3030d778684fa18112cd51b29c135f
Source noteuspto-grants-2012_11