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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8261Erstellt: 23. Oktober 2026

o-Toluenesulfonyl chloride → 7-(3-Chloro-propylsulfanyl)-4-(2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinoline

https://huagongshe.com/de/reaction/8261

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukto-Toluenesulfonyl chlorideHCID 8623—
EduktSodium BicarbonateHCID 516892—
Edukt3-[4-(2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinolin-7-ylsulfanyl]-propan-1-olHCID 21992537—
LösungsmittelPyridineHCID 1049—
Produkt7-(3-Chloro-propylsulfanyl)-4-(2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinolineHCID 10159156—

Reaktionsschritte

To a solution of Preparation #21, 3-[4-(2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinolin-7-ylsulfanyl]-propan-1-ol (25.0 mg, 0.062 mmol) in dry pyridine (0.1 mL) is added toluene sulfonyl chloride (60.0 mg, 0.31 mmol) and the resulting mixture stirred at room temperature for 72 h. Saturated sodium bicarbonate solution is added and the resulting solution extracted with ethyl acetate. The organic layer is washed with brine, dried (sodium sulfate), filtered, and concentrated in vacuo. Purification of the residue on SiO2 (5% to 10% methanol in dichloromethane) gives the desired product, 11.2 mg (43%). MS ES+ m/e 421.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087626B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-cb9b6c262d904ba286a664c696baaedc
Quellennotizuspto-grants-2006_08