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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578916Generated: October 30, 2026

1,2-Dichloroethane → HCID 60736795, compound

https://huagongshe.com/reaction/578916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant6-Chloronicotinic acidHCID 79222—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Aminomethyl)benzonitrileHCID 82608—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 60736795HCID 6073679563.8%

Reaction Steps

Combined 6-chloronicotinic acid (1.0 g, 6.35 mmol), 4-(aminomethyl)benzonitrile (1.007 g, 7.62 mmol), and EDC (1.825 g, 9.52 mmol) in methylene chloride (50 mL) then added Hunig's base (2.328 mL, 13.33 mmol) and the mixture stirred at 20° C. for 2 h. More 4-(aminomethyl)benzonitrile (250 mg), EDC (750 mg) and Hunig's base (1 mL) was added and stirring continued for 2 days. The reaction was concentrated in vacuo to give a residue which was taken up in EtOAc (100 mL) and washed with saturated aqueous ammonium chloride (100 mL) and brine, dried over magnesium sulfate and concentrated in vacuo to give a residue which was purified on an 80 g silica gel column eluted with 0 to 80% EtOAc in hexanes to give the title compound (1.1 g, 63.8% yield) as a white solid. MS m/z 272, 274 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ ppm 4.58 (d, J=6.1 Hz, 2 H) 7.53 (d, J=8.6 Hz, 2H) 7.68 (dd, J=8.3, 0.8 Hz, 1 H) 7.77-7.85 (m, 2 H) 8.28 (dd, J=8.3, 2.5 Hz, 1 H) 8.89 (dd, J=2.5, 0.5 Hz, 1 H) 9.40 (t, J=5.7 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040522B2
Source datasetuspto-grants-2015_05
ORD IDord-161acdd5d53f4bee8461ffd29b49243e
Source noteuspto-grants-2015_05