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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402524Generated: November 1, 2026

Ethyl oxoacetate → HCID 178472741, compound

https://huagongshe.com/reaction/402524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl oxoacetateHCID 70211—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178511690HCID 178511690—
SolventMethanolHCID 887—
ProductHCID 178472741HCID 178472741—

Reaction Conditions

Temperature60 °C

Reaction Steps

300 mg (0.91 mmol) of 6-cis-(4-amino-cyclohexyloxy)-7-chloro-2H-isoquinolin-1-one (12) were dissolved in 20 ml of methanol and treated with 258 mg (1.14 mmol) glyoxylic acid ethyl ester following the general method for reductive amination reactions. To achieve complete conversion, additional 5.0 equivalents of glyoxylic acid ethyl ester and 0.5 equivalents sodium cyano borohydride were added portionwise over 34 h and the temperature was increased to 60° C. after 5 h reaction time until the reaction went to completion. After filtration, the reaction solution was evaporated. The residue was dissolved in dichloromethane, washed with 1 N NaOH and saturated NaCl-solution, dried over MgSO4 and evaporated. The so obtained crude product was used in the next reaction without further purification. Rt=0.81 min (Method C). Detected mass: 365.4 (M+H+, methyl ester, because methanol was used as solvent), 0.87 min. (Method C). Detected mass: 379.4 (M+H+, ethyl ester, title compound).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742116B2
Source datasetuspto-grants-2014_06
ORD IDord-989dd939e7fd47eb9feaaac0d188485f
Source noteuspto-grants-2014_06