N-bromobutanimide → 7-Bromo-2-methyl-4-benzoxazolamine

HRID 2378429Notes

Reaction equation

HRID 2378429 reaction equation
[NH2:1][C:2]1[C:7]2[N:8]=[C:9]([CH3:11])[O:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.[Br:12]N1C(=O)CCC1=O>CN(C=O)C>[NH2:1][C:2]1[C:7]2[N:8]=[C:9]([CH3:11])[O:10][C:6]=2[C:5]([Br:12])=[CH:4][CH:3]=1

Participants

4

Reactant 2

HCID 67184N-bromobutanimideHCID 106068972-Methyl-1,3-benzoxazol-4-amine

Product 1

HCID 218751637-Bromo-2-methyl-4-benzoxazolamineYield 56.3%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
-5 °C

Procedure

Compound 474B (3.90 g, 26.3 mmol) was dissolved in DMF (45 mL) and cooled to −5° C. and N-bromosuccinimide (4.68 g, 26.3 mmol) was added in small portions and the reaction stirred for 5 h. The mixture was poured into 150 mL of ice water to give a cream colored solid which was filtered, washed with water, dissolved in CH2Cl2, dried over MgSO4, filtered and concentrated in vacuo. Purification of the crude material by flash chromatography on silica gel eluting with 20% ether/CH2Cl2 gave compound 474C (3.36 g, 56%) as a beige solid. HPLC: 95.4% at 2.583 min (retention time) (YMC S5 ODS column, 4.6×50 mm, eluting with 10-90% aqueous methanol over 4 mincontaining 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm). MS (ES): m/z 228.03 [M+H]+.

Workup

  1. customto give a cream colored solid which
  2. filtrationwas filtered
  3. washwashed with water
  4. dissolutiondissolved in CH2Cl2
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customPurification of the crude material by flash chromatography on silica gel eluting with 20% ether/CH2Cl2

Sources & evidence

ORD record
ord-9a088e26e9614aa1bdedce6d00d667c4
Source dataset
uspto-grants-2008_12
Patent number
US07470797B2

Reaction notes

Loading…