HCID 19815428, compound → HCID 19815310, compound

HRID 847032Notes

Reaction equation

HRID 847032 reaction equation
[Cl:1][C:2]1[N:3]=[C:4]([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[N:5]([CH2:9][C:10]2[CH:15]=[CH:14][C:13]([N+:16]([O-])=O)=[CH:12][CH:11]=2)[C:6]=1[CH2:7][OH:8]>CCO.C(O)(=O)C.[Fe]>[NH2:16][C:13]1[CH:12]=[CH:11][C:10]([CH2:9][N:5]2[C:6]([CH2:7][OH:8])=[C:2]([Cl:1])[N:3]=[C:4]2[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])=[CH:15][CH:14]=1

Participants

5

Procedure

To a solution of 4-chloro-2-heptyl-5-hydroxymethyl-1-(4-nitrobenzyl)imidazole (1.00 g, 2.7 mmol) in EtOH (30 mL) and glacial acetic acid (5 mL) was added iron powder (2.5 g, 44.8 mmol). The mixture was stirred while being refluxed for 20 minutes. The solution was cooled, the iron was removed by filtration, and the solution was partitioned between EtOAc and 20% aq. K2CO3 (150 mL each). The organic phase was washed with saturated aqueous NaCl, dried (MgSO4), filtered and concentrated to afford 0.8 g yellow-orange oil. Flash chromatography (silica gel, 25 g; EtOAc/hexanes, 1:1) gave 0.74 g (80%) of yellow-orange oil. NMR (200 MHz, CDCl3) δ6.80-6.60 (ABq, 4H, 7 Hz, 32 Hz); 5.10 (s, 2H); 4.45 (s, 2H); 3.75-3.60 (m, 2H); 2.55 (t, 2H, 5 Hz); 1.75-1.65 (m, 2H); 1.30-1.15 (m, 8H); 0.90-0.80 (m, 3H). Mass Spec. 335.

Workup

  1. temperaturewhile being refluxed for 20 minutes
  2. temperatureThe solution was cooled
  3. customthe iron was removed by filtration
  4. customthe solution was partitioned between EtOAc and 20% aq. K2CO3 (150 mL each)
  5. washThe organic phase was washed with saturated aqueous NaCl
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-f3ec3ac027134fa7b0902da3ea230849
Source dataset
uspto-grants-1992_08
Patent number
US05138069

Reaction notes

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