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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925477Generated: October 28, 2026

Benzaldehyde → HCID 67519559, compound

https://huagongshe.com/reaction/1925477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantTrifluoroacetateHCID 84468—
Reactant1-(4-aminobutyl)-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 18783953—
ReactantHCID 67519397HCID 67519397—
ProductHCID 67519559HCID 67519559—

Reaction Steps

The compounds in the table below were prepared and purified according to the methods of Parts B and C of Examples 246-257 using 1-(4-benzylaminobutyl)-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-4-amine in lieu of 2-methoxymethyl-1-{4-[(pyridin-3-ylmethyl)amino]butyl}-1H-imidazo[4,5-c]quinolin-4-amine. 1-(4-Benzylaminobutyl)-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-4-amine was prepared according to the general method of Part A of Examples 246-257 using benzaldehyde in lieu of pyridine 3-carboxaldehyde and 1-(4-aminobutyl)-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-4-amine in lieu of 1-(4-aminobutyl)-2-methoxymethyl-1H-imidazo[4,5-c]quinolin-4-amine. The table below shows the reagent used for each example, the structure of the resulting compound, and the observed accurate mass for the isolated trifluoroacetate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178677B2
Source datasetuspto-grants-2012_05
ORD IDord-670d22e7650d45b1b1dcbbc30fc2da3a
Source noteuspto-grants-2012_05