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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57637Generated: October 26, 2026

2-(Methyl(4-(trimethylstannyl)phenyl)amino)ethanol → (R)-tert-butyl 2-((7-(4-((2-hydroxyethyl)(methyl)amino)phenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/57637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methyl(4-(trimethylstannyl)phenyl)amino)ethanolHCID 71093669—
Reactant(R)-tert-butyl 2-((7-chloropyrido[4,3-b]pyrazin-5-ylamino)methyl)morpholine-4-carboxylateHCID 86706988—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product(R)-tert-butyl 2-((7-(4-((2-hydroxyethyl)(methyl)amino)phenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)morpholine-4-carboxylateHCID 86717398—

Reaction Steps

2-(methyl(4-(trimethylstannyl)phenyl)amino)ethanol (223 mg, 0.713 mmol), (R)-tert-butyl 2-((7-chloropyrido[4,3-b]pyrazin-5-ylamino)methyl)morpholine-4-carboxylate (246 mg, 0.648 mmol), tetrakis(triphenylphosphine)palladium (150 mg, 0.13 mmol) was mixed in toluene, reacted at 100° C. overnight. Then it was filtrated and concentrated, purified by flash chromatography (PE: EA=2:1 to 1:1) to give crude product as a reddish-brown oil. And it was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434726B2
Source datasetuspto-grants-2016_09
ORD IDord-8adadb20d68244eca3ec8c74e7a4b1cf
Source noteuspto-grants-2016_09