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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622318Generated: November 1, 2026

Hydrochloric Acid → HCID 178516633, compound

https://huagongshe.com/reaction/1622318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant5-[3-(N-hydroxyamidino)phenyl]-1H-naphtho[1,2-b][1,4]diazepin-2,4(3H,5H)-dioneHCID 178513308—
SolventAcetonitrileHCID 6342—
ProductHCID 178516633HCID 17851663342.6%

Reaction Steps

To an ice-cold solution of 5-[3-(N-hydroxyamidino)phenyl]-1H-naphtho[1,2-b][1,4]diazepin-2,4(3H,5H)-dione (310 mg, 0.94 mmol) and 1,8-diazabicyclo[5,4,0]-7-undecene (561 □L, 3.75 mmol) in acetonitrile (5.7 mL) was added dropwise, a solution of thiocarbonyldiimidazole (251 mg, 1.41 mmol) in acetonitrile (6 mL). The mixture was stirred at room temperature for 1.5 hours, to which was added 1M hydrochloric acid, and extracted with chloroform. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1˜0/1), to give the titled compound (161 mg, yield 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778933B2
Source datasetuspto-grants-2014_07
ORD IDord-308754ae0b3b4984b40bcd7f10faa36f
Source noteuspto-grants-2014_07