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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394177Generated: November 2, 2026

Water → HCID 59681779, compound

https://huagongshe.com/reaction/1394177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-N,N-diethylethanamineHCID 70608—
Reactant4-[2-(4-Amino-furazan-3-yl)-imidazo[4,5-c]pyridin-1-yl]-phenolHCID 57721189—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59681779HCID 5968177917%

Reaction Steps

To a solution containing 50 mg the product from Example 38 (0.17 mmols) in 3.4 mL of dry DMF was added 14 mg of NaH (0.34 mmols, 60% suspension in oil). After stirring at ambient temperature for 5 min, 44 mg of 2-bromoethyl-diethylamine (0.17 mmols) was added to the reaction. The reaction was warmed to 60° C. for 16 h. After cooling to room temperature, 1 mL of water was carefully added to the reaction mixture. The mixture was diluted with 20 mL of EtOAc and washed with 2N NaOH (3×10 mL). The organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The residue was dissolved in a minimum volume of DMSO and filtered through a 0.45 m acrodisc filter. The resulting solution was purified on the Gilson reverse-phase HPLC. The resulting product was dissolved in a minimum amount of MeOH and treated with excess 1 N HCl in diethylether. The resulting precipitate was collected and washed with diethylether to afford the title product (11 mg, 17%). MS (ES+) m/e 393 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348339B2
Source datasetuspto-grants-2008_03
ORD IDord-b6e9e8ebcbcb4c5781c0458c504dd4df
Source noteuspto-grants-2008_03