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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907972Generated: October 31, 2026

Diethyl Ether → HCID 67052389, compound

https://huagongshe.com/reaction/1907972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
ReactantN-HydroxyphthalimideHCID 10665—
ReactantHCID 67052438HCID 67052438—
SolventDimethylformamideHCID 6228—
ProductHCID 67052389HCID 6705238972.4%

Reaction Steps

A solution of 7-bromo-2-(chloromethyl)-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-4-amine (7.65 g, 20.8 mmol) in DMF (20 mL) was added dropwise via addition funnel to a solution of N-hydroxyphthalimide (4.07 g, 25.0 mmol) and triethylamine (4.3 mL, 31.2 mmol) in DMF (20 mL). The addition funnel was rinsed with DMF (20 mL) and the rinse was added to the reaction solution, which was stirred at room temperature. After 30 minutes, a precipitate formed. The viscous mixture was stirred at room temperature overnight, then diethyl ether (150 mL) was added. The solid was isolated by filtration, washed with diethyl ether, and dried under vacuum to provide 7.44 g of 2-{[4-amino-7-bromo-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]methoxy}-1H-isoindole-1,3(2H)-dione, which contained some triethylamine hydrochloride. The filtrate was concentrated to yield 8.5 g of a brown oil, which was found to contain product and was combined with the material from above and used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598192B2
Source datasetuspto-grants-2013_12
ORD IDord-a8fb83cf20aa4115aff551fa8928864e
Source noteuspto-grants-2013_12