3,5-Dibromo-4-methylpyridin-2-amine → 3-Bromo-4-methylpyridin-2-amine

HRID 1782580

Reaction equation

HRID 1782580 reaction equation
[Br:1][C:2]1[C:3]([NH2:10])=[N:4][CH:5]=[C:6](Br)[C:7]=1[CH3:8].[Li]CCCC>C1COCC1>[Br:1][C:2]1[C:3]([NH2:10])=[N:4][CH:5]=[CH:6][C:7]=1[CH3:8]

Participants

4

Conditions

Temperature
-78 °C

Procedure

To a solution of 3,5-dibromo-4-methyl-pyridin-2-ylamine (3.38 g, 12.7 mmol) in THF (60 mL) cooled to −78° C. was added n-BuLi (1.9M in pentane) (13.4 mL, 25.4 mmol) to give an orange solution. The solution was stirred at −78° C. for 1 h and then quenched with water (10 mL). The pH of the mixture was adjusted to ˜12 with 10N NaOH and then extracted with CH2Cl2 (3×30 mL), dried (Na2SO4), filtered and concentrated in vacuo to give an orange oil. Purification by column chromatography on silica gel (Et2O) afforded 3-bromo-4-methyl-pyridin-2-ylamine (1.68 g, 71%) as a pale yellow solid. 1H NMR (CDCl3) δ 2.32 (s, 3H), 5.00 (br s, 2H), 6.52 (d, 1H, J=6.0 Hz), 7.84 (d, 1H, J=6.0 Hz).

Workup

  1. customto give an orange solution
  2. customquenched with water (10 mL)
  3. extractionextracted with CH2Cl2 (3×30 mL)
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customto give an orange oil
  8. customPurification by column chromatography on silica gel (Et2O)

Sources & evidence

ORD record
ord-66b8ab9f484d48448421cd75e67fabc9
Source dataset
uspto-grants-2009_03
Patent number
US07498346B2

Linked notes

Loading…