4-Bromo-3-methylaniline → HCID 59254888, compound

HRID 639362Notes

Reaction equation

HRID 639362 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

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

  1. temperaturewas refluxed overnight
  2. concentrationThe resultant mixture was concentrated
  3. 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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