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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606097Generated: October 30, 2026

2-Ethyl-1-{[3-(4-fluorophenyl)isoxazol-5-yl]methyl}-N,N-bis(4-methoxybenzyl)-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-4-amine → 2-ethyl-1-{[3-(4-fluorophenyl)isoxazol-5-yl]methyl}-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-4-amine

https://huagongshe.com/reaction/606097

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethyl-1-{[3-(4-fluorophenyl)isoxazol-5-yl]methyl}-N,N-bis(4-methoxybenzyl)-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-4-amineHCID 67041307—
SolventTrifluoroacetic acidHCID 6422—
Product2-ethyl-1-{[3-(4-fluorophenyl)isoxazol-5-yl]methyl}-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-4-amineHCID 5902668442.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere, a solution of 2-ethyl-1-{[3-(4-fluorophenyl)isoxazol-5-yl]methyl}-N,N-bis(4-methoxybenzyl)-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-4-amine (2.52 g, 4.16 mmol) in trifluoroacetic acid (25 g) was stirred at room temperature for 20 hours. The trifluoroacetic acid was removed under reduced pressure, and the resulting red oil was stirred with aqueous hydrochloric acid (25 mL of 6 N) and ethanol (10 mL) for 30 minutes. The resulting mixture filtered to remove a solid impurity, cooled to 0° C., adjusted to pH 14 with the addition of 50% (w/w) aqueous sodium hydroxide, and stirred at for 30 minutes. A solid was present and was isolated by filtration and purified by sequential trituration with toluene, trituration with diethyl ether, and recrystallization from acetonitrile to provide 0.6488 g of 2-ethyl-1-{[3-(4-fluorophenyl)isoxazol-5-yl]methyl}-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-4-amine as a white flocculant solid, mp 255.0-256.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915281B2
Source datasetuspto-grants-2011_03
ORD IDord-a2f5a92b03dc44368a92485ba6c93370
Source noteuspto-grants-2011_03