Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992619Generated: October 31, 2026

Hydrazine → HCID 68539374, compound

https://huagongshe.com/reaction/1992619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantHCID 68539763HCID 68539763—
SolventEthanolHCID 702—
ProductHCID 68539374HCID 68539374135%

Reaction Steps

Anhydrous hydrazine (94 mg, 2.96 mmol) was added to 2-[4-(4-amino-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-1-yl)butoxy]-1H-isoindole-1,3(2H)-dione (600 mg, 1.48 mmol) in ethanol (25 mL) at ambient temperature. The reaction was stirred overnight, and additional hydrazine (2 equivalents) was added. After stirring for 2 hours at ambient temperature, the reaction was concentrated under reduced pressure. The residue was diluted with dichloromethane and concentrated under reduced pressure three times to remove the hydrazine and then dried under vacuum to provide 550 mg of impure 1-[4-(aminooxy)butyl]-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-4-amine as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648997B2
Source datasetuspto-grants-2010_01
ORD IDord-6089199b34b24d29a8c553382a019f96
Source noteuspto-grants-2010_01