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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678429Generated: October 31, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 59447751, compound

https://huagongshe.com/reaction/1678429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant2-(Trifluoromethyl)benzylamineHCID 76447—
ReactantHCID 67338599HCID 67338599—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59447751HCID 5944775126.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1-[4-(methylamino)-6-(4-methyl-1-piperazinyl)-1,3,5-triazin-2-yl]-3-piperidinecarboxylic acid (0.18 g, 0.55 mmol, 1.0 equiv), [(2-trifluoromethyl-phenyl)methyl]amine (0.12 g, 0.68 mmol, 1.25 equiv), and dimethylaminopyridine (DMAP, 14 mg, 0.11 mmol, 0.2 equiv) in CH2Cl2 and DMF was cooled to ˜0° C. using an ice bath. Next EDCI (0.16 g, 0.82 mmol, 1.5 equiv) was added. The reaction mixture was stirred at 0° C. for 30 min and at room temperature for an additional 2 hours. The reaction was monitored by HPLC. The solution was then diluted with CH2Cl2 and washed with saturated aqueous NaCl. The organic layer was dried over Na2SO4, and concentrated to provide the crude product. The crude product was dissolved in methanol and purified by HPLC to afford 73 mg of the title compound. MS (ES+): m/e 493.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008483B2
Source datasetuspto-grants-2011_08
ORD IDord-c19d30ef7319403a97377f76a536fe51
Source noteuspto-grants-2011_08