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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559158Generated: October 31, 2026

Hydrazine, ethyl-, ethanedioate (1:1) → 5-[3-(2,4-Dichlorophenyl)-1,9-dimethyl-2-oxo-2,9-dihydro-1H-pyrido[2,3-b]indol-6-yl]-1-ethyl-1H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/559158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine, ethyl-, ethanedioate (1:1)HCID 96181—
Reactant4-[3-(2,4-Dichlorophenyl)-1,9-dimethyl-2-oxo-2,9-dihydro-1H-pyrido[2,3-b]indol-6-yl]-2,4-dioxobutyric acid ethyl esterHCID 66997457—
SolventEthanolHCID 702—
Product5-[3-(2,4-Dichlorophenyl)-1,9-dimethyl-2-oxo-2,9-dihydro-1H-pyrido[2,3-b]indol-6-yl]-1-ethyl-1H-pyrazole-3-carboxylic acid ethyl esterHCID 66998072—

Reaction Steps

930 mg (1.85 mmol) of compound A 4-[3-(2,4-dichlorophenyl)-1,9-dimethyl-2-oxo-2,9-dihydro-1H-pyrido[2,3-b]indol-6-yl]-2,4-dioxobutyric acid ethyl ester are dissolved in 20 ml of absolute ethanol. 583 mg (5.56 mmol) of ethylhydrazine oxalate are added and the mixture is refluxed overnight. The reaction medium is evaporated to dryness and the residue is triturated in a saturated K2CO3 solution. The product is filtered and washed with water. Purification is carried out on a silica column, elution being carried out with EtOAc.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063061B2
Source datasetuspto-grants-2011_11
ORD IDord-cbc6c97aad13497791a1a4e340aeecef
Source noteuspto-grants-2011_11