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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 535387Erstellt: 24. Oktober 2026

Dicyclohexylcarbodiimide → tert-butyl-N-[1-[[5-bromo-6-(2-phenylethynyl)pyridin-2-yl]amino]-1-oxo-propan-2-yl]-N-methylcarbamate

https://huagongshe.com/de/reaction/535387

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt2-(((Tert-butoxy)carbonyl)(methyl)amino)propanoic acidHCID 4436857—
EduktHCID 86694367HCID 86694367—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-butyl-N-[1-[[5-bromo-6-(2-phenylethynyl)pyridin-2-yl]amino]-1-oxo-propan-2-yl]-N-methylcarbamateHCID 86694372—

Reaktionsschritte

A mixture of 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid (36 g, 177 mmol) and N,N′-dicyclohexylcarbodiimide (22.5 g, 109 mmol) in DCM (150 ml) is stirred with ice bath cooling for 30 minutes. A solution of 5-bromo-6-(2-phenylethynyl)pyridin-2-amine B2a (20 g, 73.2 mmol) in DCM (100 ml) is added. After stirring for 7 days at RT the reaction mixture is diluted with DCM and extracted with water. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by NP chromatography. Yield: 25 g (74%). HPLC-MS: M+H=458/460; tR=2.33 min (*Method—1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859541B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-d0dda53cdc214083ae398d2e611f12cf
Quellennotizuspto-grants-2014_10