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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375597Generated: November 3, 2026

Triethylamine → HCID 67214572, compound

https://huagongshe.com/reaction/1375597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiethyl cyanophosphonateHCID 76257—
ReactantSodium BicarbonateHCID 516892—
Reactant4-((4-Methylpiperazin-1-yl)methyl)anilineHCID 3153996—
ReactantHCID 10039959HCID 10039959—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67214572HCID 67214572—

Reaction Conditions

Temperature60 °C

Reaction Steps

Diethylcyanophosphonate (Aldrich, Buchs, Switzerland; 0.50 mL, 3.0 mmol) is added to a stirred mixture of 3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-benzoic acid (438 mg, 1.5 mmol), 4-[(4-methyl-1-piperazinyl)methyl]benzeneamine (308 mg, 1.5 mmol) and triethylamine (840 μL, 3.0 mmol) in 10 mL N,N-dimethylformamide at 10° C. After stirring for 12 hours at 60° C., the mixture is treated with an aqueous solution of sodium hydrogen carbonate and extracted three times with ethyl acetate. The combined extracts are washed with water, and the solvent is evaporated off under reduced pressure to give a residue. The residue is resuspended in water and filtered to afford the crude product which is recrystallised from tetrahydrofuran-ethyl acetate to give N-[3-[[4-(3-Pyridinyl)-2-pyrimidinyl]amino]-N-[(4-methyl-1-piperazinyl)-methyl]benzamide as a crystalline solid, m.p. 220–224° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169791B2
Source datasetuspto-grants-2007_01
ORD IDord-57c2a69b6f2744c5be062ea588287333
Source noteuspto-grants-2007_01