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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1845951Erstellt: 24. Oktober 2026

tert-Butyl piperazine-1-carboxylate → 6-(4-Tert-butoxycarbonylpiperazin-1-ylsulfonyl)isoquinoline

https://huagongshe.com/de/reaction/1845951

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt6-AminoisoquinolineHCID 588991—
EduktIsoquinoline-6-sulfonyl chlorideHCID 55280287—
Edukt6-(Piperazin-1-ylsulfonyl)isoquinoline dihydrochlorideHCID 66727131—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
Produkt6-(4-Tert-butoxycarbonylpiperazin-1-ylsulfonyl)isoquinolineHCID 66727209—

Reaktionsschritte

0.5 mL of triethylamine and 0.5 g of tert-butoxycarbonylpiperazine were added with stirring at room temperature to a dichloromethane solution (100 mL) of 6-chlorosulfonylisoquinoline (Reference Compound 2) synthesized according to Reference Example 2 from 500 mg of 6-aminoisoquinoline (Reference Compound 1), and reacted for 6 hours. After the completion of reaction, the reaction solution was washed with saturated saline and dried over anhydrous sodium sulfate. After concentration, the obtained crude product was purified by silica gel column chromatography (ethyl acetate:hexane=1:1) to obtain 150 mg of the compound of interest as a white crystal (23%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08951997B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-8a2892f9f65e4e048d3b0bd54c64f953
Quellennotizuspto-grants-2015_02