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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1845953Erstellt: 26. Oktober 2026

Triethylamine → (S)-6-{3-(tert-butoxycarbonylamino)pyrrolidin-1-ylsulfonyl}isoquinoline

https://huagongshe.com/reaction/1845953

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt(3S)-(-)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514396—
EduktIsoquinoline-6-sulfonyl chlorideHCID 55280287—
Edukt(R)-6-(3-aminopyrrolidin-1-ylsulfonyl)isoquinoline dihydrochlorideHCID 66727170—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-6-{3-(tert-butoxycarbonylamino)pyrrolidin-1-ylsulfonyl}isoquinolineHCID 66727094—

Reaktionsschritte

A dichloromethane solution (100 mL) of 6-chlorosulfonylisoquinoline (Reference Compound 2) was added with stirring at room temperature to a solution containing 423 mg of (S)-(−)-3-(tert-butoxycarbonylamino)pyrrolidine dissolved in 20 mL of dichloromethane further supplemented with 0.5 mL of triethylamine, and reacted for 6 hour. The reaction solution was washed with saturated saline and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated, and the obtained crude product was purified by silica gel column chromatography (acetone:hexane=1:2) to obtain 560 mg of the compound of interest as a colorless oil (65%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08951997B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-de958c0ddf41474598828c5ca6db4c47
Quellennotizuspto-grants-2015_02