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HRID 988596作成日:2026年10月25日

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

https://huagongshe.com/reaction/988596

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
反応物Methanesulfonic AcidHCID 6395—
反応物QuinolineHCID 7047—
反応物1-(Pyridin-4-yl)pyrrolidin-3-olHCID 21906198—
反応物2-amino-N-(5-chloropyridin-2-yl)benzamideHCID 21906381—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物N-(5-Chloropyridin-2-yl)-2-[[1-(4-pyridinyl)pyrrolidin-3-yloxycarbonyl]amino]benzamideHCID 2190635732.8%

反応手順

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 quinoline (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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06635657B1
出典データセットuspto-grants-2003_10
ORD IDord-57330204374a45c9a659e73a357b3a1b
出典メモuspto-grants-2003_10