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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 730265Erstellt: 23. Oktober 2026

Dimethylformamide → HCID 10215266, Verbindung

https://huagongshe.com/de/reaction/730265

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktMethyl iodideHCID 6328—
Edukt5-NitroindoleHCID 22523—
EduktAluminum chloride, hexahydrateHCID 24564—
EduktSodium hydrideHCID 24758—
Edukt1-methyl-1H-indol-5-amineHCID 2769564—
KatalysatorZincHCID 23994—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 10215266HCID 10215266—

Reaktionsschritte

1-Methylindole-5-ylamine. To a round-bottomed flask was added 5-nitroindole (0.81 g, 5.0 mmol, Aldrich) and anhydrous DMF (40 mL). The solution was stirred magnetically and treated with sodium hydride (0.40 g, 10 mmol, 60% dispersion in mineral oil, Aldrich) followed by iodomethane (0.71 gm 10 mmol, Aldrich). Stirring was continued at 25° C. for 30 min, then the reaction mixture was quenched by the addition of water (75 mL) and extracted with EtOAc. The organic extract was concentrated in vacuo to provide a crude residue. Analogous to the procedure of Goswami, P.; Chowdhury, P.; Indian J Chem, Sect B, 1997, 36 (2), 185-186, the crude residue was dissolved in THF (40 mL) and added to Zn dust (0.22 g, 3.3 mmol, Aldrich) and AlCl3.6H2O (4.78 g, 19.8 mmol, Aldrich) in water (1 mL), magnetically stirred at 25° C. The reaction mixture was stirred at 25° C. for 16 h, then filtered. The filtrate was added to cold water (300 mL) and extracted with CH2Cl2 (3×100 mL). The combined organic extract was concentrated in vacuo to provide the title product. MS (ESI, pos. ion) m/z: 147 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07582657B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-70abe405ac5845be852549a871decb30
Quellennotizuspto-grants-2009_09