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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232102Generated: November 2, 2026

2-Aminothiazole → HCID 54716315, compound

https://huagongshe.com/reaction/2232102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantHCID 85585358HCID 85585358—
SolventTolueneHCID 1140—
ProductHCID 54716315HCID 5471631567.1%

Reaction Steps

A solution of 4.08 g of 2-aminothiazole and 8.0 g of 1,2-dihydro-4-hydroxy-1-phenyl-3-quinolinecarboxylic acid, ethyl ester in 250 ml of toluene was refluxed for 30 hours in a soxhlet apparatus containing 10 g of 4 Å molecular sieves. Evaporation of the volatiles afforded a residue which was purified by means of high pressure liquid chromatography (silica gel: 1:25 ethyl acetate-dichloromethane as the eluent). The resulant solution was degassed and evaporated. Recrystallization of the residue from diethyl ether yielded 6.35 g (67%) of 1,2-dihydro-4-hydroxy-1-phenyl-N-(2-thiazolyl)-3-quinolinecarboxamide, m.p. 220° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04786644
Source datasetuspto-grants-1988_11
ORD IDord-13d58314597e4d92a43af69a820f2b1a
Source noteuspto-grants-1988_11