Dimethylformamide → HCID 22320437, compound

HRID 497910Notes

Reaction equation

HRID 497910 reaction equation
S(Cl)([Cl:3])=O.[CH2:5]([C:9]1[N:10]([CH2:23][CH2:24]O)[C:11]2[C:20]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[N:14]=[C:13]([NH2:21])[C:12]=2[N:22]=1)[CH2:6][CH2:7][CH3:8].CN(C)C=O>C1(C)C=CC=CC=1>[CH2:5]([C:9]1[N:10]([CH2:23][CH2:24][Cl:3])[C:11]2[C:20]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[N:14]=[C:13]([NH2:21])[C:12]=2[N:22]=1)[CH2:6][CH2:7][CH3:8]

Participants

5

Procedure

Thionyl chloride (3.8 g, 32 mmol) was added to a solution of 2-butyl-1-(2-hydroxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine (3.7 g, 13 mmol) in toluene containing a catalytic amount of N,N-dimethylformamide. The reaction mixture was heated to reflux and then capped. When analysis by high performance liquid chromatography indicated that the reaction was complete, the reaction mixture was concentrated under reduced pressure. The residue was dissolved in warm methanol and then combined with concentrated ammonium hydroxide (5 mL). The mixture was chilled. The resulting precipitate was isolated by filtration, washed with cold methanol and then dried under vacuum overnight to provide 3.01 g of 2-butyl-1-(2-chloroethyl)-1H-imidazo[4,5-c]quinolin-4-amine as a brown solid.

Workup

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux
  3. customcapped
  4. concentrationthe reaction mixture was concentrated under reduced pressure
  5. dissolutionThe residue was dissolved in warm methanol
  6. temperatureThe mixture was chilled
  7. customThe resulting precipitate was isolated by filtration
  8. washwashed with cold methanol
  9. customdried under vacuum overnight

Sources & evidence

ORD record
ord-cef01d4f9c2b41298ebcaed5f18848f2
Source dataset
uspto-grants-2005_09
Patent number
US06949649B2

Reaction notes

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