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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384836Generated: November 1, 2026

7-Chloro-1-(hydroxymethyl)-5-methyl-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indol-4-one → 7-Chloro-5-methyl-4-oxo-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxaldehyde

https://huagongshe.com/reaction/1384836

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-1-(hydroxymethyl)-5-methyl-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indol-4-oneHCID 15461901—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product7-Chloro-5-methyl-4-oxo-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxaldehydeHCID 1546190287.9%

Reaction Steps

5.7 g (65.6 mmol) of manganese dioxide are added to a solution of 3.3 g (9.7 mmol) of 7-chloro-1-(hydroxymethyl)-5-methyl-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indol-4-one in 300 ml of dichloromethane and the reaction mixture is stirred for 24 hours at reflux. The mixture is cooled and filtered through a Teflon® membrane, the solid is rinsed with dichloromethane and then the filtrate is concentrated under reduced pressure. 2:88 g (8.53 mmol) of compound are isolated in the form of a white solid which is used as is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262045B1
Source datasetuspto-grants-2001_07
ORD IDord-bb62aa34eaff4ed0a317470191b64e71
Source noteuspto-grants-2001_07