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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 715486Erstellt: 24. Oktober 2026

L-Alaninol → N-((S)-1-hydroxypropan-2-yl)-2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-4-carboxamide

https://huagongshe.com/de/reaction/715486

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktL-AlaninolHCID 80307—
Eduktphenyl 2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-4-carboxylateHCID 89875412—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-((S)-1-hydroxypropan-2-yl)-2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-4-carboxamideHCID 8987455452%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of phenyl 2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-4-carboxylate (20 mg, 0.042 mmol, Intermediate-91, single enantiomer) and (S)-2-aminopropan-1-ol in THF (1.0 mL) is heated at 90° C. overnight. The reaction mixture is concentrated. The residue is purified by preparative LC-MS to give 9.9 mg (52% yield) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09187475B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-7ceb700fbfbb4ff9b1fdcf5ff47e3e80
Quellennotizuspto-grants-2015_11