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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 552206Erstellt: 26. Oktober 2026

Methane → 6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-beta-carbolin-8-ylamine

https://huagongshe.com/reaction/552206

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
EduktAmmonium ChlorideHCID 25517—
Edukt[2-(6-chloro-8-nitro-9H-beta-carbolin-7-ylsulfanyl)-ethyl]-dimethyl-amineHCID 67166181—
KatalysatorIronHCID 23925—
LösungsmittelEthanolHCID 702—
LösungsmittelEthyl AcetateHCID 8857—
Produkt6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-beta-carbolin-8-ylamineHCID 67164517107%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A 50 ml round-bottom flask with a magnetic stirrer was charged with [2-(6-chloro-8-nitro-9H-β-carbolin-7-ylsulfanyl)-ethyl]-dimethyl-amine (106 mg, 0.30 mmol) in 8 ml of anhydrous ethanol. To the resulting orange mixture at RT was added 0.33 M aqueous ammonium chloride (1.95 ml, 0.64 mmol) and iron powder (540 mg, 9.67 mmol). The reaction mixture was heated to 60° C. and stirred vigorously for 20 hr. Next, the mixture was cooled to RT, diluted with ethyl acetate (20 ml) and activated charcoal (ca. 150 mg) was added. The resulting mixture was filtered through a pad of celite and the resulting filtrate concentrated to afford 103 mg of 6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-β-carbolin-8-ylamine as a yellow solid. The crude product was used directly in the coupling step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07951801B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-867bd3fb01d946509767c125250c1e0f
Quellennotizuspto-grants-2011_05