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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225502Generated: October 25, 2026

Triethylamine → 4-[(3-Oxo-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]benzamide

https://huagongshe.com/reaction/225502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantPropylphosphoric anhydrideHCID 16167369—
Reactant4-((3-Oxopiperazin-1-yl)methyl)benzoic acidHCID 16777099—
ReactantN-(3-amino-4-methylphenyl)-4-(pyridin-3-yl)-2-pyrimidine-amineHCID 24820369—
SolventDimethylformamideHCID 6228—
Product4-[(3-Oxo-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]benzamideHCID 10217696—

Reaction Steps

A solution of propylphosphonic anhydride in N,N-dimethylformamide (Fluka, Buchs, Switzerland; 1.3 mL of 50%, 2.25 mmol) is added dropwise to a stirred mixture of 4-methyl-N-[4-(3-pyridinyl)-2-pyrimidinyl]-1,3-benzenediamine (416 mg, 1.5 mmol), 4-[(3-oxo-1-piperazinyl)methyl]benzoic acid (351 mg, 1.5 mmol) and triethylamine (1.7 mL, 12 mmol) in dry N,N-dimethylformamide (4 mL). The mixture is stirred for 17 hours at room temperature and then treated with saturated aqueous sodium hydrogen carbonate solution (100 mL). The resulting precipitate is filtered, washed with water, dried and recrystallised from methanol to give the title compound as a cream crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557105B2
Source datasetuspto-grants-2009_07
ORD IDord-c3e61f6688dc4d85bd0d7f3e4111673b
Source noteuspto-grants-2009_07