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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875103Generated: October 31, 2026

1,2-Dichloroethane → HCID 178436403, compound

https://huagongshe.com/reaction/1875103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68487595HCID 68487595—
Reactant2-azido-4-chloro-1H-imidazole-5-carboxylic acidHCID 178514530—
CatalystLindlars catalystHCID 131709914—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178436403HCID 17843640353.5%

Reaction Steps

A solution of 3-{[3-(aminomethyl)-6-ethyl-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.075 g, 0.246 mmol), 2-azido-4-chloro-1H-imidazole-5-carboxylic acid (0.051 g, 0.271 mmol), EDC (0.052 g, 0.271 mmol) and HOBT (0.041 g, 0.271 mmol) in DMF (4 ml) was stirred at RT under an atmosphere of nitrogen for 16 h then ethyl acetate (100 mL) and saturated aqueous NaHCO3 solution (100 mL) were added. The organic layer was separated, washed with saturated aqueous NaHCO3 solution (100 mL), water (100 mL), dried over MgSO4, filtered and concentrated. Ethyl acetate (20 mL) and Lindlar Catalyst (0.026 g, 0.247 mmol) were added and the mixture was stirred at RT under an atmosphere of hydrogen (55 psig) for 19 h. The vessel was carefully vented and the mixture was filtered thru Celite, concentrated purified by Reverse Phase HPLC (MeCN/water+0.1% TFA) to give the title compound (0.059 g, 51%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 10.93 (s, 1H), 7.77 (t, 1H), 7.70 (t, 1H), 7.39 (s, 1H), 7.33 (t, 1H), 7.18-7.29 (m, 2H), 5.81 (s, 2H), 4.47 (d, 2H), 2.47-2.54 (m, 2H), 1.08 (t, 3H). LCMS m/z 450.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-8fffd20813c0484385012115ad9f9977
Source noteuspto-grants-2012_11