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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383156Generated: October 31, 2026

1,1,1-Trimethoxypropane → HCID 86626166, compound

https://huagongshe.com/reaction/2383156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-TrimethoxypropaneHCID 141145—
ReactantPyridinium chlorideHCID 10176127—
ReactantTert-butyl [4-(3-amino-7-benzyloxyquinolin-4-ylamino)butyl]carbamateHCID 68900070—
SolventTolueneHCID 1140—
ProductHCID 86626166HCID 86626166206.3%

Reaction Steps

tert-Butyl[4-(3-amino-7-benzyloxyquinolin-4-ylamino)butyl]carbamate (20.7 g, 43.6 mmol) was dissolved in toluene (225 mL). Pyridine hydrochloride (2.03 g) and trimethyl orthopropionate (6.2 mL, 43.6 mmol) were added, and the mixture was heated at reflux for 3.25 hours. The reaction was allowed to cool to room temperature; a fine precipitate formed. The precipitate was isolated by filtration and washed with toluene. The off-white solid was allowed to dry for 2 hours under vacuum. The filtrate was evaporated, and the residue was dissolved in dichloromethane. The resulting solution was washed with water and brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford a brown amorphous solid. The solids were combined to provide 17.2 g of tert-butyl[4-(7-benzyloxy-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263594B2
Source datasetuspto-grants-2012_09
ORD IDord-e8b2532cc9934afbb845aa568daa4a1d
Source noteuspto-grants-2012_09