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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968549Generated: October 29, 2026

Ethyl cyanoacetate → HCID 49788129, compound

https://huagongshe.com/reaction/1968549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodiumHCID 5360545—
Reactant1-(2-aminopyrimidin-4-yl)-2-bromoethanoneHCID 11600964—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 49788129HCID 4978812937%

Reaction Steps

Ethylcyanoacetate (5.3 mL, 0.05 mol) was added to a suspension of sodium metal (1.15 g, 0.05 mol) in 150 mL of anhydrous EtOH at 0° C. After sodium dissolution the reaction mixture was concentrated and the resultant solid was added to a solution of 1-(2-amino-pyrimidin-4-yl)-2-bromo-ethanone (15 g, 0.05 mol) in 300 mL of anhydrous THF and diisopropylethylamine (8.8 mL, 0.05 mol). The reaction mixture was stirred overnight at rt, concentrated and the residue was suspended in water and extracted with DCM. The organic extracts were dried (Na2SO4) and concentrated. The crude was purified by flash chromatography (DCM/MeOH 95:5) to give 4.5 g (37%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426417B2
Source datasetuspto-grants-2013_04
ORD IDord-955a8b5efadd43a6b25542e9dbc6a55f
Source noteuspto-grants-2013_04