Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241455Generated: November 2, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 178481066, compound

https://huagongshe.com/reaction/2241455

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-MethylpiperazineHCID 53167—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant4-(3-Formylphenoxy)butanoic acidHCID 16495682—
Reactant3-[4-(4-Methyl-piperazin-1-yl)-4-oxo-butoxy]-benzaldehydeHCID 57480928—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178481066HCID 17848106662%

Reaction Steps

3-[4-(4-Methyl-piperazin-1-yl)-4-oxo-butoxy]-benzaldehyde. To a solution of 4-(3-formyl-phenoxy)-butyric acid (981 mg, 4.72 mmol, 1.0 equiv) and N-methylpiperazine (576 mg, 5.19 mmol, 1.1 equiv) in dichloromethane at 0° C. was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDCI; 1.18 g, 6.14 mmol, 1.3 equiv) and 1-hydroxybenzotriazole hydrate (HOBT; 701 mg, 5.19 mmol, 1.1 equiv). The reaction mixture, which was allowed to warm to rt, was stirred for 2.0 h and then poured into water. This mixture was extracted three times with ethyl acetate. The combined extracts were dried (Na2SO4), filtered, and concentrated under reduced pressure. The crude residue was purified by column chromatography (silica gel, 5% MeOH in dichloromethane) to afford 847 mg (62%) of the desired product. 1H NMR (400 MHz, CD3OD): 9.72 (s, 1H), 7.29-7.23 (m, 2H), 7.22-7.19 (m, 1H), 7.05-6.98 (m, 1H), 3.87 (t, J=6.1 Hz, 2H), 3.43-3.31 (m, 4H), 2.39 (t, J=7.2 Hz, 2H), 2.27-2.17 (m, 4H), 2.08 (s, 3H), 1.92-1.80 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723359B2
Source datasetuspto-grants-2010_05
ORD IDord-9497df1a540c4021a6f19279c0d69526
Source noteuspto-grants-2010_05