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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415084Generated: October 26, 2026

Water → N-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-2,5-dimethyl-1-pyrrolidine carboxamide

https://huagongshe.com/reaction/1415084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant2,5-DimethylpyrrolidineHCID 96034—
Reactant2-Chloro-6-(4-isothiocyanatophenoxy)pyridineHCID 21391418—
ProductN-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-2,5-dimethyl-1-pyrrolidine carboxamideHCID 21391448—

Reaction Steps

2,5-Dimethylpyrrolidine (2.5 grams; 0.0284 mole) was added at ambient temperature to a solution of 4-((6-chloro-2-pyridinyl)oxy)phenyl isothiocyanate, prepared as in Example 7 (7.0 grams; 0.0284 moles) in 25 ml. of dry pyridine. The resulting reaction mixture was allowed to stand at ambient temperatures for a period of about 16 hours and then poured into 300 ml. of cold water. The resulting product precipitate was recovered by filtration, washed with water and taken up in boiling benzene. Hexane was then added to the solution and the solution cooled to precipitate the desired N-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-2,5-dimethyl-1-pyrrolidine carboxamide compound as a crystalline solid having a carbon, hydrogen, nitrogen and chlorine content of 62.2, 5.7, 11.9 and 10.2 percent, respectively, as compared with contents of 62.5, 5.82, 12.5 and 10.25 percent, respectively, calculated for the named structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04003733
Source datasetuspto-grants-1977_01
ORD IDord-a13b716af532402bb5bb9efb014fa8f6
Source noteuspto-grants-1977_01