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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360759Generated: November 1, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 25235304, compound

https://huagongshe.com/reaction/1360759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
Reactant3-Amino-2-methoxypyridineHCID 2737488—
Reactant2-(2,6-Dichloro-phenyl)-3H-benzoimidazole-5-carboxylic acid hydrazideHCID 57786585—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 25235304HCID 25235304—

Reaction Steps

Combine 2-methoxy-3-amino-pyridine (75 mg, 0.606 mmol) and di-imidazol-1-yl-methanethione (108 mg, 0.606 mmol) in DMF (1.5 mL) and stir for 7.5 hr. Add 2-(2,6-dichloro-phenyl)-3H-benzoimidazole-5-carboxylic acid hydrazide (150 mg, 0.466 mmol) and DMF (1 mL). Stir for 3 days. Add EDCI (179 mg, 0.932 mmol) and heat to 80° C. for 1 hr. Upon cooling, dilute the reaction with EtOAc (75 mL) and extract with water (15 mL). Dry the organic phase over Na2SO4 and evaporate the solvent. Purify the residue by reverse phase HPLC (35-50% ACN/H2O+5 mM NH4OH) to afford the title compound as a light tan solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 3.98 (s, 3H) 7.07 (dd, J=7.77, 4.99 Hz, 1H) 7.62-7.68 (m, 1H) 7.72 (d, J=1.89 Hz, 1H) 7.70 (s, 1H) 7.74-7.92 (m, 3H) 8.00-8.23 (m, 1H) 8.42 (dd, J=7.83, 1.64 Hz, 1H) 10.12 (br. s., 1H) 13.30 (br. s., 1H); MS m/z=452.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879850B2
Source datasetuspto-grants-2011_02
ORD IDord-ca842f7163954967af7b7a1f9d528960
Source noteuspto-grants-2011_02