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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507492Generated: November 1, 2026

Cesium carbonate → HCID 117678052, compound

https://huagongshe.com/reaction/1507492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant5-Fluoro-1,3-benzothiazoleHCID 18786167—
ReactantHCID 117677347HCID 117677347—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 117678052HCID 117678052—

Reaction Steps

DMF (4.3 mL) was added to a 125 mL round-bottom flask containing 5-fluorobenzo[d]thiazole (268 mg, 1.749 mmol). Compound 23 (420 mg, 0.874 mmol), Pd(Ph3P)4 (202 mg, 0.175 mmol), Cs2CO3 (1709 mg, 5.25 mmol) and CuI (33.3 mg, 0.175 mmol) were then added. The mixture was degassed placed in an oil bath that was preheated to 100° C. for 1 h. The reaction mixture was cooled to room temperature, diluted with water and ethyl acetate and filtered through celite. The organics were then separated and the water layer was washed with ethyl acetate. The organics were combined, washed with brine (×3), dried over sodium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel, eluting with EtOAc/hexane to give the title compound as a white solid. 1H NMR (CDCl3) δ 10.81-10.78 (m, 1H), 7.79-7.75 (m, 1H), 7.62-7.59 (m, 1H), 7.11-7.07 (m, 1H), 4.41-4.89 (m, 1H), 4.16-4.14 (m, 2H), 3.69-3.44 (m, 2H), 2.00-1.25 (m, 13H), LCMS 3.30 min, 506 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221809B2
Source datasetuspto-grants-2015_12
ORD IDord-925e6b14a4d347b997627ffb634d95f2
Source noteuspto-grants-2015_12