Ammonia → HCID 22254492, compound

HRID 967068Notes

Reaction equation

HRID 967068 reaction equation
Cl[C:2]1[C:11]2[N:12]=[CH:13][N:14]([CH2:15][CH:16]([CH3:19])[CH2:17][OH:18])[C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:3]=1.[OH-].[K+].[NH3:22]>>[NH2:22][C:2]1[C:11]2[N:12]=[CH:13][N:14]([CH2:15][CH:16]([CH3:19])[CH2:17][OH:18])[C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:3]=1

Participants

4

Procedure

R 3-(4-Chloro-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-1-ol (1.0 g, 3.6 mmol) and methanolic ammonia (30 mL of ˜15%) were combined and then heated in a steel bomb at 150° C. The container was allowed to cool to ambient temperature. Excess methanolic potassium hydroxide was added to the reaction mixture which was then concentrated under reduced pressure to decrease the volume. Water was added and then concentration was continued until a solid formed. The solid was isolated by filtration, washed with water and then dried to provide a near white solid. This material was recrystallized from methanol/dichloromethane to provide R 3-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-1-ol as colorless solid, m.p. 258-261° C. Analysis: Calculated for C14H16N4O: % C, 65.61, % H, 6.29; % N, 21.86. Found: % C, 65.50, % H, 6.3, % N, 21.7.

Workup

  1. concentrationwas then concentrated under reduced pressure
  2. additionWater was added
  3. concentrationconcentration
  4. customformed
  5. customThe solid was isolated by filtration
  6. washwashed with water
  7. customdried
  8. customto provide a near white solid
  9. customThis material was recrystallized from methanol/dichloromethane

Sources & evidence

ORD record
ord-d031293ba5a54c3288890b32e896626b
Source dataset
uspto-grants-2005_10
Patent number
US06953804B2

Reaction notes

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