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HRID 1617Erstellt: 23. Oktober 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → N-Carboxy-[1-butyl-4-piperidinylmethyl]-carbazole

https://huagongshe.com/de/reaction/1617

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
EduktN-Carboxy-[1-butyl-4-piperidinylmethyl]-1,2,3,4,4a,9a-hexahydrocarbazoleHCID 67817506—
LösungsmittelChloroformHCID 6212—
ProduktN-Carboxy-[1-butyl-4-piperidinylmethyl]-carbazoleHCID 19691861—

Reaktionsschritte

N-Carboxy-[1-butylpiperidin-4-ylmethyl]-1,2,3,4,4a,9a-hexahydrocarbazole (0.530 g, 1.32 mmol) was dissolved in chloroform (25 ml) and treated with 2,3-dichloro-5,6-dicyano-1, 4-benzoquinone (0.329 g, 1.58 mmol) with stirring. The mixture was heated to reflux for 12 hours, cooled, and more 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (0.329 g 1.58 mmol) added with stirring. The mixture was heated to reflux for 12 hours, cooled and evaporated under reduced pressure. The residue was purified by Silica-gel chromatography, eluting with 2%MeOH/CHCl3 to give the title compounds as 3:1 mixture. The mixture was separated by preparative HPLC using a Waters Micro Bondapak C18 (300 mm×7.8 mm) column and eluting with 75:25 MeCN: 0.1M Ammonium Acetate (pH 5.0).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726187
Quelldatensatzuspto-grants-1998_03
ORD IDord-4f6016db03934931aac4c3c4d6a66417
Quellennotizuspto-grants-1998_03