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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158661Generated: November 3, 2026

Pyridine → 3-[(RS)-1-(5-Chloro-pyridin-2-yloxy)-ethyl]-4-(3,4-dichloro-phenyl)-pyrrolidine-1-carbonyl chloride

https://huagongshe.com/reaction/1158661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantTriphosgeneHCID 94429—
Reactant5-Chloro-2-{(RS)-1-[(3SR,4RS)-4-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-ethoxy}-pyridineHCID 66999184—
SolventDichloromethaneHCID 6344—
Product3-[(RS)-1-(5-Chloro-pyridin-2-yloxy)-ethyl]-4-(3,4-dichloro-phenyl)-pyrrolidine-1-carbonyl chlorideHCID 86628180249%

Reaction Steps

To a stirred solution of carbonic acid ditrichloromethyl ester (triphosgene) (22 mg, 0.074 mmol) in CH2Cl2 (3 mL) at −78° C., was added a solution of 5-chloro-2-{(RS)-1-[(3SR,4RS)-4-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-ethoxy}-pyridine (intermediate XV-B-2) (70 mg, 0.19 mmol) and pyridine (0.033 mL, 0.41 mmol) in CH2Cl2 (2 mL) over 30 minutes. The temperature was raised to RT, and stirring was continued over night. The organic phase was washed with H2O, dried over Na2SO4. Concentration under vacuo yielded and column chromatography (SiO2, EtOAc/H, 1:1) yielded 80 mg (98%) of the title compound as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812021B2
Source datasetuspto-grants-2010_10
ORD IDord-7c00a1bac14c4b59830672ee3c655397
Source noteuspto-grants-2010_10