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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360872Generated: October 26, 2026

Potassium Fluoride → N-[4-methyl-5-(3-thienyl)-1,3-thiazol-2-yl]acetamide

https://huagongshe.com/reaction/1360872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant4,4,5,5-Tetramethyl-2-(thiophen-3-yl)-1,3,2-dioxaborolaneHCID 2760597—
ReactantN-(5-Iodo-4-methyl-2-thiazolyl)acetamideHCID 57417074—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductN-[4-methyl-5-(3-thienyl)-1,3-thiazol-2-yl]acetamideHCID 1199359266%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a microwave tube, N-(5-iodo-4-methyl-1,3-thiazol-2-yl)acetamide, Intermediate 1 (564.2 mg; 2 mmol; 1 eq) and Pd(dppf)Cl2 (73.2 mg; 0.10 mmol; 0.05 eq) are suspended in Toluene (7 ml). A solution of potassium fluoride (464.8 mg; 8 mmol; 4 eq) in MeOH (7 ml) is added. 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene (630.3 mg; 3 mmol; 1.50 eq) is finally added as a solid. The resulting solution is flushed with argon, the tube is closed and heated under microwave action at 120° C. for 15 minutes. The reaction mixture is filtered over Celite and the solvents are evaporated. The resulting crude product is dissolved in EtOAc, washed with water and brine and dried over MgSO4. It is then purified by preparative HPLC, affording the title compound as white-off solid (316.7 mg; 66% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879888B2
Source datasetuspto-grants-2011_02
ORD IDord-ccf3eacb5e914cfc8305ec894d642762
Source noteuspto-grants-2011_02