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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 873370Erstellt: 26. Oktober 2026

1,2-Dichloroethane → N-((4,6-Dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-6-(trifluoromethyl)-1H-indole-4-carboxamide

https://huagongshe.com/reaction/873370

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
Edukt4-MethylmorpholineHCID 7972—
EduktHOAtHCID 181649—
Edukt3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridin-2-oneHCID 7063844—
Edukt1-Isopropyl-6-(trifluoromethyl)-1H-indole-4-carboxylic acidHCID 67464224—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktN-((4,6-Dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-6-(trifluoromethyl)-1H-indole-4-carboxamideHCID 6746815065,4%

Reaktionsschritte

To a solution of 1-(1-methylethyl)-6-(trifluoromethyl)-1H-indole-4-carboxylic acid (40 mg, 0.147 mmol) in dimethyl sulfoxide (1 mL) were added 3-(aminomethyl)-4,6-dimethyl-2(1H)-pyridinone (41.7 mg, 0.221 mmol), N-methylmorpholine (0.065 mL, 0.590 mmol), 1-hydroxy-7-azabenzotriazole (40.1 mg, 0.295 mmol) and EDC (56.5 mg, 0.295 mmol), and the mixture was stirred overnight. The mixture was quenched with water (5 mL) and stirred for 10 min. The precipitate was collected by filtration and dried under high vacuum to give the title compound (39 mg, 63%) as an off-white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.47 (m, 6 H), 2.13 (s, 3 H), 2.23 (s, 3 H), 4.36 (d, J=5.05 Hz, 2 H), 4.99 (dt, J=13.20, 6.66 Hz, 1 H), 5.89 (s, 1 H), 6.98 (d, J=3.03 Hz, 1 H), 7.68 (s, 1 H), 7.86 (d, J=3.28 Hz, 1 H), 8.08 (s, 1 H), 8.45 (t, J=4.93 Hz, 1 H), 11.56 (s, 1 H). MS: (M+H)+=406.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08975291B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-b69a0b99ce154452867e508ac9d87d9f
Quellennotizuspto-grants-2015_03