Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761124Generated: October 26, 2026

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

https://huagongshe.com/reaction/1761124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactantmethyl((1-methyl-1H-indol-2-yl)methyl)amineHCID 11401058—
Reactant(E)-3-(6-aminopyridin-3-yl)2-methylacrylic acid HCl saltHCID 67343937—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
Product(E)-3-(6-aminopyridin-3-yl)-2-methyl-N-methyl-N-(1-methyl-1H-indol-2-ylmethyl)acrylamideHCID 5744085375%

Reaction Steps

To a stirred solution of (E)-3-(6-aminopyridin-3-yl)2-methylacrylic acid HCl salt (0.5 g, 2.3 mmole) in dry 1:1 DMF/CH2Cl2 (30 mL) at RT was added 1-methyl-2-(methylaminomethyl)indole (0.42 g, 2.4 mmole), HOBt H2O (0.32 g, 2.4 mmole), Et3N (0.66 mL, 4.7 mmole), and EDC (0.46 g, 2.4 mmole). After stirring for 24 hr the reaction was concentrated to dryness. The residue was taken up in ethyl acetate and the solution was washed with H2O, dried (Na2SO4), and concentrated under vacuum. Flash chromatography on silica gel (4% methanol/CHCl3) followed by trituration with ethyl acetate/hexane gave the title compound (0.55 g, 75%) as an off-white solid: LCMS (ES) m/e 335.2 (M+H)+; 1H NMR (300 MHz, DMSO-dV 8 7.96 (s,1H), 7.52 (d, J=7.8 Hz, 1 H), 7.48 (dd,1H), 7.43 (d, J=7.8 Hz,1H), 7.14 (t,1H), 7.03 (t, 1H), 6.46 (d, J=8.7 Hz, 1H), 6.43 (s,1H), 6.40 (s,1H), 6.17 (br s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846819B1
Source datasetuspto-grants-2005_01
ORD IDord-1e069a5e2fcc4d15ab1c5e0856b3b56a
Source noteuspto-grants-2005_01