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HRID 77421Erstellt: 24. Oktober 2026

Methyl iodide → N-((S)-6-Bromo-1,2,3,4-tetrahydronaphthalen-2-yl)-N-methyl-5-cyclopropylmethoxy-pyridine-2-carboxamide

https://huagongshe.com/de/reaction/77421

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktBromomethylcyclopropaneHCID 81503—
Edukt5-Hydroxypyridine-2-carboxylic acidHCID 268740—
Edukt(2S)-6-Bromo-1,2,3,4-tetrahydronaphthalen-2-amineHCID 22831536—
ProduktN-((S)-6-Bromo-1,2,3,4-tetrahydronaphthalen-2-yl)-N-methyl-5-cyclopropylmethoxy-pyridine-2-carboxamideHCID 66663511—

Reaktionsschritte

According to method G, (S)-6-bromo-1,2,3,4-tetrahydronaphthalen-2-ylamine was coupled with 5-hydroxypyridine-2-carboxylic acid and the product was then alkylated on the phenolic hydroxyl function with bromomethylcyclopropane according to method a Finally, the amide function was alkylated according to method B with methyl iodide. The product was thus obtained with the molecular weight of 415.33 (C21H23BrN2O2); MS (ESI): 415 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841290B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-88d81b669a224bbfa615843c2afeea02
Quellennotizuspto-grants-2014_09