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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384834Generated: November 1, 2026

Water → Ethyl 7-chloro-5-methyl-4-oxo-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxylate

https://huagongshe.com/reaction/1384834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantPhenylhydrazineHCID 7516—
ReactantEthyl 6-chloro-2-(ethoxycarbonyl)-1-methyl-oxo-1h-indole-3-acetateHCID 15461899—
SolventAcetic AcidHCID 176—
ProductEthyl 7-chloro-5-methyl-4-oxo-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxylateHCID 1546190078.7%

Reaction Steps

4 ml (40.6 mmol) of phenylhydrazine are added at room temperature to a solution of 4.6 g (13.6 mmol) of ethyl 6-chloro-2-(ethoxycarbonyl)-1-methyl-α-oxo-1H-indole-3-acetate in 120 ml of acetic acid. The reaction mixture is stirred for 30 min at room temperature and then for 4 hours at reflux. The mixture is cooled and 350 ml of dichloromethane and 100 ml of water are added. The organic phase is separated by settling, washed with a saturated aqueous sodium hydrogencarbonate solution and then with water, dried over sodium sulphate, filtered and concentrated under reduced pressure and the residue is purified by chromatography on a column of silica gel. 4.1 g (10.7 mmol) of product are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262045B1
Source datasetuspto-grants-2001_07
ORD IDord-4f5d4fe14ecc4053bf96cea59d22a4a1
Source noteuspto-grants-2001_07