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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400283Generated: November 1, 2026

Hydrochloric Acid → HCID 178487105, compound

https://huagongshe.com/reaction/2400283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
ReactantSodium AzideHCID 33557—
Reactant6-(5-Methoxy-2-phenylindol-1-ylmethyl)pyridine-2-carbonitrileHCID 86707935—
CatalystZinc bromideHCID 10421208—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 178487105HCID 17848710582.2%

Reaction Steps

To a mixture of 6-(5-methoxy-2-phenylindol-1-ylmethyl)pyridine-2-carbonitrile (95 mg), isopropyl alcohol (6 mL), and water (4 mL) were added sodium azide (36 mg) and zinc bromide (32 mg). This mixture was stirred overnight while heated to reflux. The reaction mixture was left to cool to room temperature, and then diluted with ethyl acetate. To the mixture was added 2 mol/L hydrochloric acid (4 mL), followed by stirring at room temperature for 30 minutes. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: dichloromethane-methanol) to obtain the title compound (88 mg). 1H-NMR (DMSO-d6) δ ppm: 3.78 (3H, s), 5.61 (2H, s), 6.54 (1H, d, J=7.8 Hz), 6.66 (1H, d, J=0.4 Hz), 6.78 (1H, dd, J=2.5, 8.9 Hz), 7.16 (1H, d, J=2.5 Hz), 7.29 (1H, d, J=8.9 Hz), 7.35-7.55 (5H, m), 7.90 (1H, t, J=7.8 Hz), 8.05 (1H, d, J=7.8 Hz). ESI-MS (m/z): 383 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796247B2
Source datasetuspto-grants-2014_08
ORD IDord-e5271f95b21947ae86ed22d13bad322d
Source noteuspto-grants-2014_08