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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875252Generated: November 1, 2026

1,2-Dichloroethane → HCID 178509907, compound

https://huagongshe.com/reaction/1875252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-{[3-(Aminomethyl)-6-bromo-2-fluorophenyl]oxy}-5-chlorobenzonitrileHCID 67197166—
Reactant4-chloro-1-({[2-(trimethylsilyl)ethyl]oxy}methyl)-1H-imidazole-5-carboxylic acidHCID 68485533—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 178509907HCID 1785099072.8%

Reaction Steps

EDC (0.028 g, 0.148 mmol) and HOBT (0.020 g, 0.148 mmol) were added to a solution of 3-{[3-(aminomethyl)-6-bromo-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.053 g, 0.148 mmol) and 4-chloro-1-({[2-(trimethylsilyl)ethyl]oxy}methyl)-1H-imidazole-5-carboxylic acid (0.041 g, 0.148 mmol) in DMF (2 mL). The mixture was stirred at RT overnight. The reaction mixture was extracted with ethyl acetate and saturated aqueous sodium bicarbonate. The organic layer was dried over sodium sulfate and concentrated to give a yellow oil which was dissolved in dichloromethane (1.5 mL). Trifluoroacetic acid (0.5 ml, 6.49 mmol) was added and the mixture was stirred at RT overnight. Purification by reverse phase HPLC (acetonitrile:water with 0.1% formic acid) gave the title compound 0.002 g, 2.5%) as a white solid. 1H NMR (400 MHz, methanol-d4) δ ppm 7.69 (s, 1H), 7.48-7.55 (m, 2H), 7.29 (t, 1H), 7.22 (d, 1H), 7.19 (s, 1H), 4.61 (s, 2H). ES MS m/z 483 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-fa3e649daf8c463f8b9a2ed5812e1a80
Source noteuspto-grants-2012_11