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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779702Generated: October 31, 2026

Methanol → HCID 15231843, compound

https://huagongshe.com/reaction/1779702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium HydroxideHCID 14923—
ReactantAmmonium formateHCID 2723923—
ReactantHCID 67758872HCID 67758872—
CatalystPalladium hydroxideHCID 9942167—
SolventHydrochloric AcidHCID 313—
ProductHCID 15231843HCID 1523184399.4%

Reaction Steps

N,N-Bis(phenylmethyl)-6,7,8,9-tetrahydro-2-methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-4-amine (820 mg, 1.87 mmole), palladium hydroxide on carbon (200 mg, Pearlman's catalyst), ammonium formate (472 mg, 7.48 mmole) and methanol (50 mL) were combined and heated at reflux for 48 hours. During the course of the reaction additional catalyst (200 mg) and ammonium formate (472 mg) were added. The reaction mixture was cooled to ambient temperature then filtered through a layer of celite. The filtrate was evaporated to provide a residue which was dissolved in 3N hydrochloric acid. The solution was made basic (pH 9) with ammonium hydroxide then extracted with methylene chloride (3×200 mL). The extracts were combined, washed with water, dried over magnesium sulfate then concentrated to provide 480 mg of a white solid. This solid was recrystallized from ethyl acetate to provide 260 mg of the desired product as a white solid, m.p. 170°-172° C. Analysis: Calculated for C15H22N4 +1/2H2O: %C, 68.16; %H, 8.64; %N, 21.2; Found: %C, 68.47; %H, 8.14; %N, 21.08.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627281
Source datasetuspto-grants-1997_05
ORD IDord-c76b1d92f80e4047af6837373a2c089e
Source noteuspto-grants-1997_05