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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420688Generated: October 31, 2026

Sodium hydride → 4-((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-{[(phenylmethyl)oxy]methyl}ethyl)-6-(methyloxy)-1,4-dihydropyrido[2,3-b]pyrazin-3(2H)-one

https://huagongshe.com/reaction/420688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactantethyl N-[2-[((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-{[(phenylmethyl)oxy]methyl}ethyl)amino]-6-(methyloxy)-3-pyridinyl]glycinateHCID 58001773—
SolventTetrahydrofuranHCID 8028—
Product4-((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-{[(phenylmethyl)oxy]methyl}ethyl)-6-(methyloxy)-1,4-dihydropyrido[2,3-b]pyrazin-3(2H)-oneHCID 6665846591%

Reaction Steps

To a solution of NaH (50.5 g, 57-63% dispersion in mineral oil, 1.26 mol) in THF (8.5 L) was added ethyl N-[2-[((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-{[(phenylmethyl)oxy]methyl}ethyl)amino]-6-(methyloxy)-3-pyridinyl]glycinate (577.8 g, 1.147 mol) at −5° C. When the addition was complete the mixture was warmed to room temperature and stirred for 30 min. The reaction was quenched by the addition of saturated aqueous NH4Cl (610 ml) and the mixture was stirred for 10 min. Na2SO4 (1 kg) was added and the mixture was stirred for 10 min before being filtered through celite. The filter cake was washed with EtOAc (5 L). The filtrate was evaporated and the dark purple oil was purification by column chromatography and mixtures of heptane and EtOAc as eluent to give 477 g (91%) of 4-((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-{[(phenylmethyl)oxy]methyl}ethyl)-6-(methyloxy)-1,4-dihydropyrido[2,3-b]pyrazin-3(2H)-one as a viscous purple oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097628B2
Source datasetuspto-grants-2012_01
ORD IDord-9e9b5ec36c7e4d20b10485ce69075b7f
Source noteuspto-grants-2012_01