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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255535Generated: October 30, 2026

Triethylamine → HCID 20183629, compound

https://huagongshe.com/reaction/255535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Aminophenylacetic acidHCID 14533—
Reactant4-Chloro-3-nitroquinolineHCID 11275808—
SolventDimethylformamideHCID 6228—
ProductHCID 20183629HCID 20183629—

Reaction Steps

Using the method of Example 1, 4-chloro-3-nitroquinoline was reacted with 4-aminophenylacetic acid in N,N-dimethylformamide in the presence of triethylamine to provide N-(3-nitro-4-quinolinyl)-4-aminophenylacetic acid. This acid was reduced using the method of Example 26 to provide N-(3-amino-4-quinolinyl)-4-aminophenylacetic acid. This diamine was then reacted with formic acid using the method of Example 137 to provide 1-(4-carboxymethylphenyl)-1H-imidazo[4,5-c]quinoline. Recrystallization from methanol provided solid of m.p. 236°-240° C. Analysis: Calculated for C18H13N3O2 : %C, 71.3; %H, 4.3; %N, 13.9; Found; %C, 70.8; %H, 4.3; %N, 13.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698348
Source datasetuspto-grants-1987_10
ORD IDord-64f16bdff78541cf848bbcca52762288
Source noteuspto-grants-1987_10