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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 887372Erstellt: 23. Oktober 2026

Diisopropylethylamine → 2-((R)-1-hydroxy-3-methylbutan-2-ylamino)-4-(5-methyl-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidine-5-carbonitrile

https://huagongshe.com/de/reaction/887372

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktD-ValinolHCID 6950587—
Edukt4-(5-methyl-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-2-(methylsulfonyl)pyrimidine-5-carbonitrileHCID 59414377—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-((R)-1-hydroxy-3-methylbutan-2-ylamino)-4-(5-methyl-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidine-5-carbonitrileHCID 5941454777%

Reaktionsschritte

A mixture of 4-(5-methyl-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-2-(methylsulfonyl)pyrimidine-5-carbonitrile (120 mg, 0.257 mmol), (R)-(−)-2-amino-3-methyl-1-butanol (57 □l, 0.515 mmol) and diisopropylethylamine (90 □l, 0.515 mmol) in THF (4 mL) was heated at reflux for 1 hour. The reaction mixture was concentrated in vacuo and the residue was purified on silica gel by flash column chromatography to give the title compound as a colourless glassy solid (97 mg, 77% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08247421B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-c4bbf42d0f464ca8afc76f02810313c6
Quellennotizuspto-grants-2012_08