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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1690382Erstellt: 26. Oktober 2026

Tri-o-tolylphosphine → (E)-3-(2-aminopyrimidin-5-yl)-N-(2-methyl-1H-indol-3-ylmethyl)-N-methylacrylamide

https://huagongshe.com/reaction/1690382

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTri-o-tolylphosphineHCID 80271—
EduktDiisopropylethylamineHCID 81531—
Edukt2-Amino-5-bromopyrimidineHCID 231310—
EduktN-(2-methyl-1H-indol-3-ylmethyl)-N-methylacrylamideHCID 22139057—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelPropionitrileHCID 7854—
Produkt(E)-3-(2-aminopyrimidin-5-yl)-N-(2-methyl-1H-indol-3-ylmethyl)-N-methylacrylamideHCID 9973366128,8%

Reaktionsschritte

A solution of N-methyl-N-(2-methyl-1H-indol-3-ylmethyl)acrylamide (1.18 g, 6.5 mmole), 2-amino-5-bromopyrimidine (0.5 g, 2.9 mmole), Pd(OAc)2 (0.11 g, 0.49 mmole), tri-ortho-tolylphosphine (0.17 g, 0.55 mmole), and diisopropylethylamine (1.5 mL, 8.6 mmole) in propionitrile (100 mL) and DMF (10 mL) was heated at reflux overnight. The dark mixture was filtered through celite®, and the filtrate was concentrated. Flash chromatography on silica gel (9:1 CHCl3/CH3OH containing 5% NH4OH) gave the title compound (1.2 g, 65%): MS (ES) m/e 372 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08153652B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-73240552b55c4c0a81b58a0d81e33871
Quellennotizuspto-grants-2012_04