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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948408Generated: October 27, 2026

Dimethylamine → N-(5-{5-[(Dimethylamino)sulfonyl]-2-thienyl}-4-methyl-1,3-thiazol-2-YL)acetamide

https://huagongshe.com/reaction/1948408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-[2-(Acetylamino)-4-methyl-1,3-thiazol-5-yl]thiophene-2-sulfonyl chlorideHCID 86622562—
SolventDimethylformamideHCID 6228—
ProductN-(5-{5-[(Dimethylamino)sulfonyl]-2-thienyl}-4-methyl-1,3-thiazol-2-YL)acetamideHCID 11998549—

Reaction Steps

5-[2-(acetylamino)-4-methyl-1,3-thiazol-5-yl]thiophene-2-sulfonyl chloride, prepared as in Step II of Example 1 (110 mg; 0.33 mmol; 1 eq), is dissolved in DMF (10 ml). Dimethylamine (0.1 ml; 1.65 mmol; 5 eq) and DIEA (0.17 ml; 0.98 mmol; 3 eq) are added. After one hour, the solvents are 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 (18) as a yellow powder (52 mg; 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399497B2
Source datasetuspto-grants-2013_03
ORD IDord-c072fdf3e4d4485bb3cd42341b9a5211
Source noteuspto-grants-2013_03