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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 516105Erstellt: 25. Oktober 2026

N,N-Diisopropylmethylamine → (R)-methyl 2-(4-chloro-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanoate

https://huagongshe.com/reaction/516105

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-DiisopropylmethylamineHCID 547370—
EduktLeucine methyl ester hydrochlorideHCID 2723695—
Edukt4,6-dichloro-2-[(2,4-dimethoxyphenyl)methyl]-7-fluoro-1H,2H,3H-pyrrolo[3,4-c]pyridin-3-oneHCID 58317575—
LösungsmittelAcetonitrileHCID 6342—
Produkt(R)-methyl 2-(4-chloro-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanoateHCID 58317585—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 4,6-dichloro-2-(2,4-dimethoxybenzyl)-7-fluoro-1H-pyrrolo[3,4-c]pyridin-3(2H)-one (3 g, 8.08 mmol), (S)-methyl 2-amino-4-methylpentanoate hydrochloride (2.94 g, 16.16 mmol), and N-isopropyl-N-methylpropan-2-amine (3.76 mL, 24.25 mmol) in ACN (50 mL) was stirred at 100° C. for 3 d. The solvent was removed and the resulting residue was used in the next step without further purification. [M+H] calc'd for C23H27ClFN3O5, 480; found, 480.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09108970B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-f841ab9bc87148b4adf520ab514a5b35
Quellennotizuspto-grants-2015_08