Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397910Generated: October 26, 2026

4-(Pyridin-2-yl)-1,3-thiazol-2-amine → 4-(N-(4-fluorophenyl)-N-methylsulfamoyl)-N-(4-(pyridin-2-yl)thiazol-2-yl)benzamide

https://huagongshe.com/reaction/1397910

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Pyridin-2-yl)-1,3-thiazol-2-amineHCID 1092459—
Reactant4-(N-(4-fluorophenyl)-N-methylsulfamoyl)benzoic acidHCID 56687146—
Product4-(N-(4-fluorophenyl)-N-methylsulfamoyl)-N-(4-(pyridin-2-yl)thiazol-2-yl)benzamideHCID 46912683—

Reaction Steps

4-(N-(4-fluorophenyl)-N-methylsulfamoyl)benzoic acid (4) (100 mg, 0.32 mmol) was treated with 4-(pyridin-2-yl)thiazol-2-amine (48 mg, 0.27 mmol) using method C. The residue was purified using flash chromatography eluting with EtOAc. The resulting solid was triturated with diethyl ether to give 4-(N-(4-fluorophenyl)-N-methylsulfamoyl)-N-(4-(pyridin-2-yl)thiazol-2-yl)benzamide as a yellow solid. Yield: 34 mg (27%). 1H-NMR: 8.61 (d, J=4.5 Hz, 1H), 8.29 (d, J=8.5 Hz, 2H), 8.02 (d, J=8.5 Hz, 1H), 7.93-7.83 (m, 2H), 7.65 (d, J=8.5 Hz, 2H), 7.36-7.31 (m, 1H), 7.24-7.12 (m, 4H), 3.17 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901306B2
Source datasetuspto-grants-2014_12
ORD IDord-01d79d445fd949739d9787997fdcb4fe
Source noteuspto-grants-2014_12