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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303309Generated: November 2, 2026

Triethylamine → 2-{[2-(Methanesulfonylamino)ethyl]amino}-4-(3-methylanilino)pyrimidine-5-carboxamide

https://huagongshe.com/reaction/2303309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(2-Aminoethylamino)-4-(m-tolylamino)pyrimidine-5-carboxamideHCID 9817349—
SolventEthyl AcetateHCID 8857—
Product2-{[2-(Methanesulfonylamino)ethyl]amino}-4-(3-methylanilino)pyrimidine-5-carboxamideHCID 18460848—

Reaction Steps

A 114 μl portion of methanesulfonyl chloride and 205 μl of triethylamine were added to a mixture of 382 mg of 2-(2-aminoethylamino)-4-(3-methylanilino)pyrimidine-5-carboxamide with 10 ml of ethyl acetate, followed by stirring at room temperature for 3.5 hours. The reaction mixture was washed with water and saturated brine, and then the organic layer was dried over anhydrous magnesium sulfate. This was concentrated under a reduced pressure and the resulting residue was recrystallized from a mixed solvent of methanol and ethyl acetate to obtain 210 mg of 2-{[2-(methanesulfonylamino)ethyl]amino}-4-(3-methylanilino)pyrimidine-5-carboxamide (colorless crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432963B1
Source datasetuspto-grants-2002_08
ORD IDord-c1d78e4fc76549d98b5f58066eee71dc
Source noteuspto-grants-2002_08