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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598293Generated: October 29, 2026

Isobutylamine → HCID 57545324, compound

https://huagongshe.com/reaction/598293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylamineHCID 6558—
ReactantPropylamineHCID 7852—
ReactantFluorobenzeneHCID 10008—
Reactant1-Fluoro-4-(methylsulphonyl)benzeneHCID 67994—
Reactant1,1,1-TrimethoxybutaneHCID 123512—
Reactant3-Methoxypropanoyl chlorideHCID 2759728—
ReactantHCID 67050950HCID 67050950—
ProductHCID 57545324HCID 57545324—

Reaction Steps

The general methods described in Parts A-G of Example 1 were used to prepare 7-benzyloxy-2-(2-methoxyethyl)-1-propyl-1H-imidazo[4,5-c]quinoline. Propylamine was used in lieu of isobutylamine in Part E, and methoxypropionyl chloride was used in lieu of trimethyl orthobutyrate in Part G. 7-Benzyloxy-2-(2-methoxyethyl)-1H-propyl-1H-imidazo[4,5-c]quinoline was treated according to the general methods described in Parts A-D of Examples 35-40. In Part B, the fluorobenzene used was 4-fluorophenyl methyl sulfone. Following chromatographic purification, the product was recrystallized from acetonitrile to provide 0.890 g of 7-(4-methanesulfonylphenoxy)-2-(2-methoxyethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-4-amine as dark tan needles, mp 210-212° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897597B2
Source datasetuspto-grants-2011_03
ORD IDord-959129b2984d4dc6a99602b3fff2708f
Source noteuspto-grants-2011_03