Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278839Generated: October 29, 2026

Ethyl oxoacetate → HCID 178516809, compound

https://huagongshe.com/reaction/2278839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl oxoacetateHCID 70211—
ReactantHCID 178512735HCID 178512735—
SolventEthanolHCID 702—
ProductHCID 178516809HCID 178516809—

Reaction Steps

22.000 g (purity 68%, approx. 52.621 mmol) of 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboximidohydrazide in 220 ml of ethanol were initially introduced, admixed dropwise with 18.265 (89.455 mmol) of ethyl oxoacetate (50% strength solution in toluene) and heated under reflux overnight. The resulting suspension was concentrated on a rotary evaporator and stirred with diethyl ether. The solid was filtered off with suction and dried under high vacuum. Further purification was effected by chromatography on silica gel (mobile phase: dichloromethane/methanol, gradient 30:1→10:1). This gave 12.07 g of the target compound (purity 69%; 49% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133191B2
Source datasetuspto-grants-2015_09
ORD IDord-93cae992da9c4f6d86d22c2472e18e3f
Source noteuspto-grants-2015_09