Ammonium Chloride → HCID 21876045, compound

HRID 1454600Notes

Reaction equation

HRID 1454600 reaction equation
[CH3:1][O:2][C:3]1[N:8]=[C:7]([NH:9][C:10]2[CH:15]=[CH:14][C:13]([CH2:16][CH2:17][OH:18])=[CH:12][CH:11]=2)[C:6]([N+:19]([O-])=O)=[CH:5][CH:4]=1.[Cl-].[NH4+]>C(O)C.O.[Fe]>[NH2:19][C:6]1[C:7]([NH:9][C:10]2[CH:15]=[CH:14][C:13]([CH2:16][CH2:17][OH:18])=[CH:12][CH:11]=2)=[N:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1

Participants

5

Procedure

A mixture of 2-{4-[(6-methoxy-3-nitro-2-pyridinyl)amino]phenyl}ethanol (step 1, 3.52 g, 12.17 mmol), iron powder (3.4 g, 60.84 mmol) and ammonium chloride (325 mg, 6.08 mmol) in ethanol/water (v/v, 2:1, 90 mL) was heated at reflux temperature for 1 h. After cooling, the catalyst was removed and the filtrate was concentrated. The residue was extracted with ethyl acetate (100 mL) and washed with water. The organic layer was dried (MgSO4), and concentrated to give 3.41 g (quant.) of the title compound as a black oil: 1H-NMR (CDCl3) δ 7.48 (2H, d, J=8.4 Hz), 7.14 (2H, d, J=8.4 Hz), 7.04 (1H, d, J=8.2 Hz), 6.75 (1H, br.s), 6.13 (1H, d, J=8.2 Hz), 3.87 (3H, s), 3.83 (2H, t, J=6.6 Hz), 2.81 (2H, t, J=6.6 Hz).

Workup

  1. temperaturewas heated
  2. temperatureat reflux temperature for 1 h
  3. temperatureAfter cooling
  4. customthe catalyst was removed
  5. concentrationthe filtrate was concentrated
  6. extractionThe residue was extracted with ethyl acetate (100 mL)
  7. washwashed with water
  8. dry with materialThe organic layer was dried (MgSO4)
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-6213be91c5b24f0194b7926d90d0f8c0
Source dataset
uspto-grants-2009_01
Patent number
US07479564B2

Reaction notes

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