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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378283Generated: October 26, 2026

Triethylamine → N-[4-(6-methylamino-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide

https://huagongshe.com/reaction/378283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantN-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamideHCID 10644414—
SolventEthanolHCID 702—
ProductN-[4-(6-methylamino-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamideHCID 5440699244%

Reaction Conditions

Temperature140 °C

Reaction Steps

0.62 g (0.00175 mol) of N-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide was dissolved in 20 ml of ethanol, treated with 1.36 g (0.0201 mol) of methylamine hydrochloride and 5.3 ml (0.038 mol) of triethylamine and stirred in an autoclave at 140° C. for 17 hours. The mixture was freed completely from solvent, the residue was partitioned in ethyl acetate/water and filtered off under suction. There was obtained 0.30 g (44%) of N-[4-(6-methylamino-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide as beige crystals; m.p. 271-274° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-5d0eb8aab86546b7be1740b9b4966b85
Source noteuspto-grants-2000_02