Reaktion #462168

Reaktionsgleichung

dry ice carbon tetrachloride

Butyllithium

dry ice acetone

N,N-bis(phenylmethyl)-1-ethoxymethyl-1H-imidazo[4,5-c]quinolin-4-amine

Formaldehyde

→

4-bis(phenylmethyl)amino-1-ethoxymethyl-1H-imidazo[4,5-c]quinolin-2-methanol

Lösungsmittel

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwas added to the reaction mixture
2. 2
   workup.WAITAfter several minutes the reaction turned to a solid mass
3. 3
   Sonstigethe ice bath was removed
4. 4
   workup.ADDITIONThe reaction was diluted with diethyl ether and water
5. 5
   SonstigeThe ether layer was separated
6. 6
   Trocknendried over magnesium sulfate
7. 7
   Einengenconcentrated under vacuum
8. 8
   SonstigeThe residue was purified by column chromatography (silica gel eluting with 10-20% ethyl acetate in hexanes v/v)

Vorschrift

Butyllithium (1.6 mL of 2.5M in hexanes, 4 mmole) was added to a chilled (dry ice/acetone bath) solution of N,N-bis(phenylmethyl)-1-ethoxymethyl-1H-imidazo[4,5-c]quinolin-4-amine (1.7 g, 4 mmole) in tetrahydrofuran. No color change was observed. The reaction mixture was warmed to -20° C. (dry ice/carbon tetrachloride) and the reaction turned red in color. Formaldehyde gas entrained in a flow of nitrogen was added to the reaction mixture. After several minutes the reaction turned to a solid mass and the ice bath was removed. The reaction mixture was allowed to warm to ambient temperature and the color of the reaction mixture changed from red to yellow. The reaction was diluted with diethyl ether and water. The ether layer was separated, dried over magnesium sulfate and then concentrated under vacuum. The residue was purified by column chromatography (silica gel eluting with 10-20% ethyl acetate in hexanes v/v) to provide 1 g of 4-bis(phenylmethyl)amino-1-ethoxymethyl-1H-imidazo[4,5-c]quinolin-2-methanol.

Quelle