Ammonia → Imiquimod
Reaction equation
Cl[C:2]1[C:11]2[N:12]=[CH:13][N:14]([CH2:15][CH:16]([CH3:18])[CH3:17])[C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:3]=1.C([NH2:21])=O.N.[OH-].[Na+]>CO>[CH3:17][CH:16]([CH2:15][N:14]1[C:10]2[C:9]3[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=3[N:3]=[C:2]([NH2:21])[C:11]=2[N:12]=[CH:13]1)[CH3:18]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 145 °C
Procedure
A mixture of 4-chloro-1-isobutyl-1H-imidazo[4,5-c]quinoline (100.0 g, 0.385 mole) and formamide (250 ml, 6.27 mole, 16.3 equiv.) was heated to 145° C. under nitrogen atmosphere. Then, ammonia (gas) (92 g, 5.29 mole, 14 equiv.) was bubbled (4-5 g per hour) into the reaction mixture at this temperature during a period of 20 hours. Then, the reaction mixture was cooled to ambient temperature and stirred at this temperature for 3 hours. A colorless solid was collected by filtration, washed with methanol (3×100 ml), water (3×100 ml) and again with methanol (3×50 ml) and dried at 50° C. under reduced pressure overnight to give a crude Imiquimod (74.1 g, 80.2% yield, purity by HPLC: 99.3%). The crude compound (74.1 g) was slurried in a boiling mixture of methanol (500 ml) and 47% aqueous sodium hydroxide solution (about 6 ml) for 4 hours. The hot mixture was filtered and the thus obtained cake was washed with methanol (3×40 ml), water (3×50 ml) and again with methanol (3×40 ml) and dried at 50° C. under reduced pressure to yield 72.2 g of Imiquimod in 77.9% yield, having a purity of 99.85% (by HPLC)
Workup
- temperatureThen, the reaction mixture was cooled to ambient temperature
- filtrationA colorless solid was collected by filtration
- washwashed with methanol (3×100 ml), water (3×100 ml) and again with methanol (3×50 ml)
- customdried at 50° C. under reduced pressure overnight
- customto give a crude Imiquimod (74.1 g, 80.2% yield, purity by HPLC: 99.3%)
- filtrationThe hot mixture was filtered
- washthe thus obtained cake was washed with methanol (3×40 ml), water (3×50 ml) and again with methanol (3×40 ml)
- customdried at 50° C. under reduced pressure
Sources & evidence
- ORD record
- ord-7d787d1ae0ea4e4b8863f0e549ed8024
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07323568B2
Reaction notes
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