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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248276Generated: October 30, 2026

Ethyl chloroformate → HCID 178473481, compound

https://huagongshe.com/reaction/2248276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178429562HCID 178429562—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 178473481HCID 17847348152%

Reaction Steps

0.45 ml (4 7 mmol) of ethylchloroformate are added dropwise over a period of 10 minutes to a solution of 1 00 g (3.5 mmol) of 6-[2-(3-aminopropyl)-1H-benzimidazol-5-yl]-4,5-dihydro -5-methyl-3(2H)-pyridazinone and 1 25 g (9.0 mmol) of potassium carbonate in 10 ml of acetone and 10 ml of water with cooling in an ice bath. After 3 hours' stirring at room temperature, the reaction mixture is filtered and the filtrate is diluted with 20 ml of water and extracted three times with 20 ml portions of dichloromethane. The combined organic phases are dried and concentrated by evaporation under vacuum and the residue is chromatographed on silica gel with dichloromethane/methanol (9:1) as solvent. The polar main fraction (Rf 0 46) yields 0.65 g (52%) of the title compound in the form of a yellowish, amorphous solid after concentration by evaporation under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039675
Source datasetuspto-grants-1991_08
ORD IDord-7dc4bf8bffcb4258b53b8f4ff9550c3d
Source noteuspto-grants-1991_08