Triethylamine → HCID 21984427, compound
Reaction equation
[CH3:1][S:2](Cl)(=[O:4])=[O:3].[NH2:6][CH2:7][CH2:8][CH2:9][CH2:10][N:11]1[C:23]2[C:22]3[CH:21]=[CH:20][C:19]([Br:24])=[CH:18][C:17]=3[N:16]=[C:15]([NH2:25])[C:14]=2[N:13]=[C:12]1[CH2:26][O:27][CH2:28][CH3:29].C(N(CC)CC)C.[OH-].[Na+]>C(Cl)(Cl)Cl.O>[NH2:25][C:15]1[C:14]2[N:13]=[C:12]([CH2:26][O:27][CH2:28][CH3:29])[N:11]([CH2:10][CH2:9][CH2:8][CH2:7][NH:6][S:2]([CH3:1])(=[O:4])=[O:3])[C:23]=2[C:22]2[CH:21]=[CH:20][C:19]([Br:24])=[CH:18][C:17]=2[N:16]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
Methanesulfonyl chloride (0.44 mL, 5.7 mmol) was added to a suspension of 1-(4-aminobutyl)-7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-4-amine (2.04 g, 5.2 mmol) and triethylamine (0.94 mL, 6.8 mmol) in chloroform (100 mL), and the reaction was stirred for four hours. Water was added; a precipitate formed. The aqueous layer was adjusted to pH 10 with the addition of 50% aqueous sodium hydroxide. The precipitate was isolated by filtration, washed with cold chloroform, and dried overnight on the filter funnel. Material from another run was added, and entire procedure was repeated to eliminate unreacted starting material. N-{4-[4-Amino-7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl]butyl}methanesulfonamide (2.95 g) was obtained as a white solid.
Workup
- customa precipitate formed
- customThe precipitate was isolated by filtration
- washwashed with cold chloroform
- customdried overnight on the filter funnel
- additionMaterial from another run was added
Sources & evidence
- ORD record
- ord-2e45af154c4a434dbd1369dfd3e515cd
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07091214B2
Reaction notes
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