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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284699Generated: October 31, 2026

Diisopropylethylamine → N-(1-benzylpyrrolidin-3-yl)-4-(propylamino)-2-((2-(pyridin-4-yl)ethyl)amino)pyrimidine-5-carboxamide

https://huagongshe.com/reaction/2284699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Benzyl-3-aminopyrrolidineHCID 2756613—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant4-(Propylamino)-2-((2-(pyridin-4-yl)ethyl)amino)pyrimidine-5-carboxylic acidHCID 90051716—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(1-benzylpyrrolidin-3-yl)-4-(propylamino)-2-((2-(pyridin-4-yl)ethyl)amino)pyrimidine-5-carboxamideHCID 9005174285.2%

Reaction Steps

To a solution of 4-(propylamino)-2-((2-(pyridin-4-yl)ethyl)amino)pyrimidine-5-carboxylic acid (A3, 90 mg) in N,N-dimethylformamide (2 mL), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (63 mg) and 1-hydroxybenzotriazole monohydrate (45 mg) were added at room temperature, and the mixture was stirred at the same temperature for 2 hours and 30 minutes. To the reaction mixture, N,N-diisopropylethylamine (153 μL) and 1-benzyl-3-aminopyrrolidine (53 mg) were added at room temperature, and the mixture was stirred at the same temperature for 2 hours. To the reaction mixture, water was added. The solid matter was taken by filtration, washed with water, and then dried under reduced pressure. The obtained solid matter was purified by basic silica gel column chromatography to obtain N-(1-benzylpyrrolidin-3-yl)-4-(propylamino)-2-((2-(pyridin-4-yl)ethyl)amino)pyrimidine-5-carboxamide (E9, 117 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-47df18c470e0418eae37bf4b9197822b
Source noteuspto-grants-2015_09