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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1247027Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1247027

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 reaction was cooled to room temperature. N-(5-Chloropyridin-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
PatentnummerUS07129245B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-48f404344ede43d0912950d1ec2ce80a
Quellennotizuspto-grants-2006_10