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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1297454Erstellt: 26. Oktober 2026

(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acid → (E)-3-(6-aminopyridin-3-yl)-N-(6-fluoro-1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamide

https://huagongshe.com/reaction/1297454

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acidHCID 10487224—
Edukt2,3-dihydro-8-(methylaminomethyl)-1H-3a-azacyclopenta[a]indeneHCID 22139048—
Edukt6-fluoro-1-methyl-3-(methylaminomethyl)-1H-indoleHCID 22139158—
Edukt(E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic Acid HydrochlorideHCID 66905305—
Produkt(E)-3-(6-aminopyridin-3-yl)-N-(6-fluoro-1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamideHCID 1024651150,1%

Reaktionsschritte

According to the procedure of Example 24, except substituting 6-fluoro-1-methyl-3-(methylaminomethyl)-1H-indole (0.11 g, 0.59 mmole) for the 2,3-dihydro-8-(methylaminomethyl)-1H-3a-azacyclopenta[a]indene, and substituting (E)-3-(6-amino-pyridin-3-yl)acrylic acid (0.098 g, 0.59 mmole) for the (E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic acid hydrochloride salt, the title compound (0.1 g, 27%) was prepared as a white powder: MS (ES) m/e 339 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07250424B2
Quelldatensatzuspto-grants-2007_07
ORD IDord-fc96c2f091f64da5aa78a243058300ca
Quellennotizuspto-grants-2007_07