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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242020Generated: October 31, 2026

Hydrazine → HCID 58914780, compound

https://huagongshe.com/reaction/2242020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Chloro-3-nitropyridin-2-ylamineHCID 2724035—
ReactantHCID 68437854HCID 68437854—
SolventEthanolHCID 702—
ProductHCID 58914780HCID 58914780—

Reaction Conditions

Temperature80 °C

Reaction Steps

Hydrazine (1.3 eq) was added to a solution of 2-{3-[4-(2,4-dichlorophenyl)-3-(4-methyl-2-oxopiperazinyl)pyrrolyl]propyl}benzo[c]azoline-1,3-dione (8) in abs. EtOH and stirred at 75° C. for 2 hours. The reaction developed a white precipitate, which was filtered. The EtOH was concentrated under reduced pressure. The residue was taken up in CH2Cl2 and the precipitate was filtered again. The organic solution was evaporated to a foam. Assuming a quantitative yield, the residue was taken up in CH3CN and DMA (4:1). Hünig's Base (1.3 eq) was added to the mixture followed by 6-chloro-3-nitro-2-pyridylamine (10) (1.2 eq). The reaction was heated to 80° C. for 2 hours until completion was determined by LC/MS. The reaction was subsequently concentrated. The residue was dissolved in EtOAc, washed with water, brine, dried (Na2SO4), filtered, and concentrated to dryness to give 1-(1-{3-[(6-amino-5-nitro(2-pyridyl))amino]propyl}-4-(2,4-dichlorophenyl)pyrrol-3-yl)-4-methylpiperazin-2-one (11). The product (11) was purified by silica column chromatography, eluting with MeOH in CH2Cl2 (5:95, v/v). After collecting the purified fractions and concentrating, light yellow foam (LC/MS m/z 519.4 MH+, 42% yield) was attained in 95% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671049B2
Source datasetuspto-grants-2010_03
ORD IDord-106fd0259351420eaf9d5019c2abc34c
Source noteuspto-grants-2010_03