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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 397063Erstellt: 24. Oktober 2026

Triethylamine → 6-Methoxy-1-[1-(1-methyl-1H-imidazole-4-sulfonyl)-piperidin-4-yl]-3,4-dihydro-isoquinoline

https://huagongshe.com/de/reaction/397063

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-methyl-1H-imidazole-4-sulfonyl chlorideHCID 2736887—
Edukt6-Methoxy-1-piperidin-4-yl-3,4-dihydro-isoquinolineHCID 18172389—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-Methoxy-1-[1-(1-methyl-1H-imidazole-4-sulfonyl)-piperidin-4-yl]-3,4-dihydro-isoquinolineHCID 1817246056,1%

Reaktionsschritte

To a stirred solution of 6-methoxy-1-piperidin-4-yl-3,4-dihydro-isoquinoline (0.094 g, 0.385 mmol) and triethylamine (0.078 g, 0.77 mmol) in CH2Cl2 (3 ml) was added 1-methyl-1H-imidazole-4-sulfonyl chloride (0.070 g, 0.385 mmol). The reaction mixture was stirred at RT under an atmosphere of N2 overnight. The reaction mixture was diluted with CH2Cl2 (10 ml) and washed with water (2×5 ml). The organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified via radial chromatography (SiO2, 1 mm, CH2Cl2 to 5% MeOH/CH2Cl2) to give the product as an oil (0.084 g, 0.216 mmol, 56% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06608203B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-88f163b020a4417a8afec3291f8f5e4c
Quellennotizuspto-grants-2003_08