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HRID 1761131Erstellt: 26. Oktober 2026

1,2-Dichloroethane → (E)-3-(6-aminopyridin-3-yl)-N-(1,2-dimethyl-1H-indol-3-ylmethyl)-N-methylacrylamide

https://huagongshe.com/reaction/1761131

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktTriethylamineHCID 8471—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
Edukt(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acidHCID 10487224—
Edukt[(1,2-dimethyl-1H-indol-3-yl)methyl](methyl)amineHCID 10877907—
LösungsmittelDMF CH2Cy2HCID 131724718—
Produkt(E)-3-(6-aminopyridin-3-yl)-N-(1,2-dimethyl-1H-indol-3-ylmethyl)-N-methylacrylamideHCID 6020893797%

Reaktionsschritte

To a stirred solution of 1,2-dimethyl-3-(methylaminomethyl)-1H-indol e (0.8 g, 4.2 mmole) in 1:1 DMF/CH2Cy2 (30 mL) at RT was added (E)-3-(6-aminopyridin-3-yl)acrylic acid (0.7 g, 4.3 mmole), Et3N (0.61 ml, 4.3 mmole), HOBt H2O (0.58 g, 4.3 mmole) and EDC (0.83 g, 4.3 mmole). After 16 h the reaction was concentrated under vacuum and the residue was taken up in EtOAc (100 mL). The solution was washed with 1.0 N Na2CO3 (100 mL) then with brine, dried (Na2SO4), and concentrated. Purification by flas h chromatography on silica gel (4% MeOv.CHCl3) followed by trituration with 1:1 Et2O/petroleum ether and drying under vacuum gave (he title compound (1.36 g, 97%) as an off-white solid: MS (ES) H+e 335.2 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06846819B1
Quelldatensatzuspto-grants-2005_01
ORD IDord-266dcd67d21e4d468ccf4b4607f45db9
Quellennotizuspto-grants-2005_01