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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244825Generated: October 31, 2026

Dimethylformamide → HCID 57657251, compound

https://huagongshe.com/reaction/244825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMorpholineHCID 8083—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 57657227HCID 57657227—
SolventWaterHCID 962—
ProductHCID 57657251HCID 57657251—

Reaction Steps

A 20-ml glass vial was charged with anhydrous DMF (1 mL), 3-[4-amino-2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]propanoic acid (165 mg, 0.43 mmol), N-(3-dimethylaminopropyl)-N″-ethylcarbodiimide hydrochloride (100 mg, 0.52 mmol, 1.3 eq), 1-hydroxybenzotriazole (70.3 mg, 0.52 mmol, 1.3 eq), and morpholine (110 mg, 1.29 mmol, 3.0 eq). The reaction was maintained at ambient temperature overnight. The reaction mixture was poured into water (10 mL), and the resulting mixture was extracted with dichloromethane (3×10 mL). The chloroform fractions were combined and concentrated, and the residue was purified by chromatography using a HORIZON HPFC system (silica cartridge, eluting with 0-30% CMA in chloroform) followed by recrystallization from acetonitrile to provide 1-[4-amino-2-(ethoxymethyl)-7-(3-morpholin-4-yl-3-oxopropyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol as a white solid, mp 118-119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658666B2
Source datasetuspto-grants-2014_02
ORD IDord-cd823ce1a8e94d6fb040373876c1b5c3
Source noteuspto-grants-2014_02