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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409968Generated: October 31, 2026

Hydroxylamine HCl → HCID 136344372, compound

https://huagongshe.com/reaction/2409968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamine HClHCID 21645—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86703287HCID 86703287—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 136344372HCID 136344372105.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of hydroxylammonium chloride (891 mg) in dimethylsulfoxide (5 mL) was added sodium hydrogen carbonate (1.29 g), and this mixture was stirred at 50° C. for 75 minutes. Then, a solution of 6-(6-methoxy-2-phenyl-1H-indol-3-ylmethyl)pyridine-2-carbonitrile (435 mg) in dimethylsulfoxide (1.4 mL) was added dropwise thereto, followed by stirring at 50° C. for 24 hours. The reaction mixture was left to be cooled and diluted with water, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to obtain the title compound (504 mg). 1H-NMR (CDCl3) δ ppm: 3.86 (3H, s), 4.40 (2H, s), 5.63 (2H, br s), 6.43-6.69 (1H, br), 6.77 (1H, dd, J=2.2, 8.8 Hz), 6.91 (1H, d, J=2.2 Hz), 7.09-7.15 (1H, m), 7.31-7.40 (2H, m), 7.40-7.49 (2H, m), 7.49-7.60 (3H, m), 7.66-7.74 (1H, m), 8.06 (1H, br s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815903B2
Source datasetuspto-grants-2014_08
ORD IDord-dba134f58b084b17aa127fe0378e624a
Source noteuspto-grants-2014_08