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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889552Generated: October 30, 2026

Hydroxylamine HCl → HCID 136052333, compound

https://huagongshe.com/reaction/1889552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamine HClHCID 21645—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59351636HCID 59351636—
SolventDimethyl SulfoxideHCID 679—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 136052333HCID 13605233355%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of hydroxylammonium chloride (0.41 g), sodium hydrogencarbonate (0.6 g) and dimethyl sulfoxide (20 mL) was stirred at 40° C. for 30 min, 4′-{[2-ethyl-6-oxo-5-(2-phenylethyl)thieno[2,3-b]pyridin-7(6H)-yl]methyl}biphenyl-2-carbonitrile (0.34 g) was added, and the mixture was stirred at 90° C. for 16 hr. The reaction mixture was diluted with chloroform, washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue obtained by silica gel column chromatography was dissolved in methylene chloride (40 mL), N,N′-carbonyldiimidazole (0.13 g) and then 1,8-diazabicyclo[5.4.0]undec-7-ene (0.11 mL) were added, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with chloroform, washed successively with saturated aqueous potassium hydrogensulfate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was recrystallized from tetrahydrofuran to give the title compound as colorless crystals (0.23 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501750B2
Source datasetuspto-grants-2013_08
ORD IDord-a88d1d08e4734b6186a020e99917ca6c
Source noteuspto-grants-2013_08