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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225130Generated: October 26, 2026

Water → 2-[4-(7-chloro-4-quinolylamino)phenyl]-N-(1-ethyl-3-piperidyl)acetamide monohydrate

https://huagongshe.com/reaction/225130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-amino-N-ethylpiperidineHCID 98094—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant2-[4-(7-Chloro-4-quinolylamino)phenyl]acetic acid hydrochlorideHCID 70597336—
SolventDimethyl SulfoxideHCID 679—
Product2-[4-(7-chloro-4-quinolylamino)phenyl]-N-(1-ethyl-3-piperidyl)acetamide monohydrateHCID 2332900492.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

7.0 Grams (0.02 mole) of 2-[4-(7-chloro-4-quinolylamino)phenyl]acetic acid hydrochloride were dissolved in 150 milliliters of dimethyl sulphoxide by heating the stirred mixture to 100° C. under nitrogen. The solution was cooled to room temperature, 6.48 grams (0.04 mole) of carbonyl di-imidazole were added and the mixture was stirred for 21/2 hours under nitrogen. 7.68 Grams (0.06 mole) of 3-amino-1-ethylpiperidine were added, the solution was stirred for another 21/2 hours and poured into 500 milliliters of water. The mixture was refrigerated overnight and the resulting solid was broken up, stirred with water, collected and dried. The solid was dissolved in chloroform and chromatographed on an alumina column made up in chloroform. Elution with chloroform/methanol (4:1) gave 8.15 grams (92.5% yield) of 2-[4-(7-chloro-4-quinolylamino)phenyl]-N-(1-ethyl-3-piperidyl)acetamide monohydrate, melting point 160°-162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235908
Source datasetuspto-grants-1980_11
ORD IDord-eb994b99a963498aa299fb5d018646e3
Source noteuspto-grants-1980_11