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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223593Generated: October 30, 2026

Ethyl Bromide → HCID 15581179, compound

https://huagongshe.com/reaction/223593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 178499160HCID 178499160—
SolventDimethylformamideHCID 6228—
ProductHCID 15581179HCID 1558117946%

Reaction Steps

To a mixture of 3.3 g (0.013 mol) of 3-carbomethoxy-4-hydroxy-7-methyl-pyrido[3',2':4,5]thieno[3,2-C]pyridazine, 3.8 g potassium bicarbonate, in 90 ml of anhydrous DMF was slowly added 9 ml of ethyl bromide and stirring was continued at 60°-70° C. for 3 hours. The solvent was then removed, the residue was diluted with water and filtered to give 3.4 g of crude product. Crystallization from EtoAc-hexane gave 1.8 g (46%) of pure 3-carbethoxy-4-ethoxy-7-methyl pyrido[3',2':4,5]thieno[3,2-C]pyridazine; m.p. 158°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355164
Source datasetuspto-grants-1982_10
ORD IDord-c71c700273384af1a1f1314b5d69b239
Source noteuspto-grants-1982_10