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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988596Generated: October 25, 2026

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

https://huagongshe.com/reaction/988596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantMethanesulfonic AcidHCID 6395—
ReactantQuinolineHCID 7047—
Reactant1-(Pyridin-4-yl)pyrrolidin-3-olHCID 21906198—
Reactant2-amino-N-(5-chloropyridin-2-yl)benzamideHCID 21906381—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductN-(5-Chloropyridin-2-yl)-2-[[1-(4-pyridinyl)pyrrolidin-3-yloxycarbonyl]amino]benzamideHCID 2190635732.8%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06635657B1
Source datasetuspto-grants-2003_10
ORD IDord-57330204374a45c9a659e73a357b3a1b
Source noteuspto-grants-2003_10