4-Bromo-3-methylaniline → HCID 59254888, compound
Reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([OH:12])[CH:8]=2)[N:3]=1.[Br:13][C:14]1[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][C:15]=1[CH3:21].C(N(C(C)C)CC)(C)C>C(O)C>[Br:13][C:14]1[CH:20]=[CH:19][C:17]([NH:18][C:2]2[CH:11]=[CH:10][C:9]3[C:4](=[CH:5][CH:6]=[C:7]([OH:12])[CH:8]=3)[N:3]=2)=[CH:16][C:15]=1[CH3:21]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The mixture containing 2-chloroquinolin-6-ol (1eq), 4-bromo3-methylaniline (2 eq) and diisopropylethylamine in ethanol (1 M) was refluxed overnight. The resultant mixture was concentrated and purified on silica gel to provide the desired product. The mixture containing 2-chloroquinolin-6-ol (1 eq), 4-bromo3-methylaniline (2 eq) and diisopropylethylamine in ethanol (1M) was refluxed overnight. The resultant mixture was concentrated and purified on silica gel to provide the desired product.
Workup
- temperaturewas refluxed overnight
- concentrationThe resultant mixture was concentrated
- custompurified on silica gel
Sources & evidence
- ORD record
- ord-73ad1b61be754d8481e1a9ec34612740
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07691866B2
Reaction notes
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