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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355082Generated: October 31, 2026

Triethylamine → N-(2-aminopyrimidin-5-yl)-2-methyl-5-(3-(trifluoromethyl)phenylsulfonamido)benzamide

https://huagongshe.com/reaction/2355082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
Reactant5-amino-N-(2-aminopyrimidin-5-yl)-2-methylbenzamideHCID 16116848—
SolventChloroformHCID 6212—
ProductN-(2-aminopyrimidin-5-yl)-2-methyl-5-(3-(trifluoromethyl)phenylsulfonamido)benzamideHCID 16118872—

Reaction Steps

To a solution of 5-amino-N-(2-aminopyrimidin-5-yl)-2-methylbenzamide 28 (85 mg, 0.349 mmol) in CHCl3 (2 mL) was added triethylamine (0.453 mmol) and 3-(trifluoromethyl)benzene-1-sulfonyl chloride (0.064 mL, 0.401 mmol). The reaction mixture was heated to reflux for 12 h, cooled to rt and concentrated in vacuo. The crude residue was adsorbed on SiO2 and purified by flash chromatography (CH2Cl2/MeOH 99:1) on SiO2 to afford N-(2-aminopyrimidin-5-yl)-2-methyl-5-(3-(trifluoromethyl)phenylsulfonamido)benzamide 29. MS m/z found 452 [MH+]; calc. for C19H16F3N5O3S=451.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754717B2
Source datasetuspto-grants-2010_07
ORD IDord-d7e7c442e49e4f5188f6f6851b0c1d5f
Source noteuspto-grants-2010_07