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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241733Generated: November 1, 2026

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

https://huagongshe.com/reaction/2241733

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 numberUS07723526B2
Source datasetuspto-grants-2010_05
ORD IDord-c8694d45420d4e64916671b19d5b1b6b
Source noteuspto-grants-2010_05