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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889549Generated: October 29, 2026

Hydroxylamine HCl → HCID 136052349, compound

https://huagongshe.com/reaction/1889549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamine HClHCID 21645—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59351691HCID 59351691—
SolventDimethyl SulfoxideHCID 679—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 136052349HCID 13605234949%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of hydroxylammonium chloride (0.43 g), sodium hydrogencarbonate (0.63 g) and dimethyl sulfoxide (20 mL) was stirred at 40° C. for 30 min, 4′-{[7-ethyl-4-(4-fluorobenzyl)-2,5-dioxo-2,3,4,5-tetrahydro-1H-thieno[2,3-e][1,4]diazepin-1-yl]methyl}biphenyl-2-carbonitrile (0.38 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 (20 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 purified by silica gel column chromatography to give the title compound as colorless crystals (0.19 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501750B2
Source datasetuspto-grants-2013_08
ORD IDord-29a39adeb8704ecbbbb1a6b6a664b340
Source noteuspto-grants-2013_08