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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1882925Erstellt: 26. Oktober 2026

Phosgene → N-(5-Chloropyridin-2-yl)-2-[[1-(4-pyridinyl)pyrrolidin-3-yloxycarbonyl]amino]benzamide

https://huagongshe.com/reaction/1882925

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosgeneHCID 6371—
EduktMethanesulfonic AcidHCID 6395—
EduktQuinolineHCID 7047—
Edukt1-(Pyridin-4-yl)pyrrolidin-3-olHCID 21906198—
Edukt2-amino-N-(5-chloropyridin-2-yl)benzamideHCID 21906381—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(5-Chloropyridin-2-yl)-2-[[1-(4-pyridinyl)pyrrolidin-3-yloxycarbonyl]amino]benzamideHCID 2190635732,8%

Reaktionsschritte

To as solution of 1-(4-pyridinyl)-3-hydroxypyrrolidine (330 mg, 2.01 mmol) in dichloromethane (30 mL) was added methanesulfonic acid (0.15 mL, 2.31 mmol). After 15 seconds, quinoline (0.3 mL, 2.54 mmol) was added, immediately followed by a toluene solution of phosgene (0.65 mL, 1.25 mmol). After 5 minutes, the reaction was placed in an oil bath at 35° C. After 45 minutes, the r action was cooled to room temperature. N-(5-Chloro-pyridin-2-yl)-2-aminobenzamide (498 mg, 2.01 mmol) was added, followed by quinolin (0.3 mL, 2.54 =mmol). After stirring overnight, the reaction was diluted with dichloromethane (150 mL) and washed with saturated aqueous sodium carbonate (2×25 mL). The organic layer was concentrated in vacuo and purified by flash column chromatography (100% CH2Cl2 to 9% MeOH/CH2Cl2) and then by HPLC to give the title product (181 mg, 0.41 mmol, 21%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06759414B2
Quelldatensatzuspto-grants-2004_07
ORD IDord-c9daee0915b54de680f8ee8a672f60d7
Quellennotizuspto-grants-2004_07