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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18343Erstellt: 23. Oktober 2026

(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acid → (E)-3-(6-aminopyridin-3-yl)-N-(4-fluoro-1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamide

https://huagongshe.com/de/reaction/18343

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—
Edukt4-fluoro-1-methyl-3-(methylaminomethyl)-1H-indoleHCID 22139151—
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-(4-fluoro-1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamideHCID 1172468837%

Reaktionsschritte

According to the procedure of Example 24, except substituting 4-fluoro-1-methyl-3-(methylaminomethyl)-1H-indole (0.2 g, 1.04 mmole) for the 2,3-dihydro-8-(methylaminomethyl)-1H-3a-azacyclopenta[a]indene, and substituting (E)-3-(6-amino-pyridin-3-yl)acrylic acid (0.17 g, 1.04 mmole) for the (E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic acid hydrochloride salt, the title compound (0.11 g, 37%) was prepared as an off-white powder: MS (ES) m/e 339 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741339B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-75c85322411c4b8fb7b4937baef98d9a
Quellennotizuspto-grants-2010_06