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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948402Generated: October 30, 2026

Water → N-(4-Methyl-5-{5-[(piperazin-1-YL)sulfonyl]-2-thienyl}-1,3-thiazol-2-YL)acetamide

https://huagongshe.com/reaction/1948402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-MethylpiperazineHCID 53167—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-[2-(Acetylamino)-4-methyl-1,3-thiazol-5-yl]thiophene-2-sulfonyl chlorideHCID 86622562—
SolventDichloromethaneHCID 6344—
ProductN-(4-Methyl-5-{5-[(piperazin-1-YL)sulfonyl]-2-thienyl}-1,3-thiazol-2-YL)acetamideHCID 11998431—

Reaction Steps

5-[2-(acetylamino)-4-methyl-1,3-thiazol-5-yl]thiophene-2-sulfonyl chloride, prepared as in Step II of Example 1 (280 mg; 0.84 mmol; 1 eq), is dissolved in DCM (10 ml). N-Methyl piperazine (1.4 g; 16.8 mmol; 20 eq) and DIEA (0.17 ml; 0.98 mmol; 3 eq) are added. After one night reaction, water (1 ml) is added and the solvents evaporated to dryness. The crude product is re-dissolved in DCM and washed with NH4Cl saturated solution, water and dried over MgSO4. After evaporation of the solvents, crude material is precipitated in a mixture of DCM and diethyl ether, affording after filtration, Compound (11) as a white solid (125 mg; 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399497B2
Source datasetuspto-grants-2013_03
ORD IDord-9a305f7c270245319f76571878e2e120
Source noteuspto-grants-2013_03