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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410568Generated: October 30, 2026

Cesium carbonate → 3-Fluoro-5-(1,3-thiazol-5-yl)aniline

https://huagongshe.com/reaction/410568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant5-BromothiazoleHCID 546059—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant3-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 59770039—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product3-Fluoro-5-(1,3-thiazol-5-yl)anilineHCID 6725650685%

Reaction Conditions

Temperature95 °C

Reaction Steps

The product of Step 1 (2.66 g, 11.22 mmol), 2-bromo-1,4-thiazole (1.003 mL, 11.22 mmol), Pd2(dba)3 (0.514 g, 0.561 mmol), X-phos (0.535 g, 1.122 mmol), and cesium carbonate (7.31 g, 22.44 mmol) were added to a dry flask. Degassed with argon, then added dioxane (25 mL) and water (2.5 mL). The reaction mixture was degassed with argon for five minutes, and then heated to 95° C. After 16 hours, the reaction mixture was cooled, diluted with ethyl acetate, filtered through celite, and concentrated. The residue was purified by column chromatography on silica gel, eluting with ethyl acetate and hexanes to afford 3-fluoro-5-(1,3-thiazol-5-yl)aniline (2.27 g, 9.49 mmol, 85%). MS ESI: [M+H]+ m/z 195.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-5c2a627510b042b8b8af3848db8c87ad
Source noteuspto-grants-2014_06