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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371616Generated: October 25, 2026

2-Chloroquinoline-4-carbonyl chloride → 2-Chloro-N-(1-cyclohexylpyrrolidin-3-yl)quinoline-4-carboxamide

https://huagongshe.com/reaction/371616

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroquinoline-4-carbonyl chlorideHCID 75438—
Reactant1-Cyclohexylpyrrolidin-3-amineHCID 3670074—
SolventChloroformHCID 6212—
Product2-Chloro-N-(1-cyclohexylpyrrolidin-3-yl)quinoline-4-carboxamideHCID 20355405—

Reaction Steps

To 3.16 gm. (0.0195 mole) of 3-amino-1-cyclohexylpyrrolidine in 50 ml. of chloroform was added dropwise a solution of 3.5 gm. (0.015 mole) of 2-chloro-4-quinolinecarbonyl chloride in 50 ml. of chloroform. The reaction mixture was concentrated under reduced pressure and the residue was partitioned between ethyl acetate containing 10% isopropyl ether and dilute hydrochloric acid. The separated acid layer was made basic with dilute sodium hydroxide solution and extracted with chloroform. The chloroform solution was dried over sodium sulfate, concentrated and the residue recrystallized twice from isopropyl ether-ethyl acetate. The product (0.7 gm.; 13%) melted at 127°-219° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087428
Source datasetuspto-grants-1978_05
ORD IDord-ab02c6ffd09e4230abcdae91bc596b11
Source noteuspto-grants-1978_05