Bromine → Imazethapyr

HRID 1029780Notes

Reaction equation

HRID 1029780 reaction equation
[C:1]([C:4]([NH:9][CH2:10][C:11]1[N:19]=[CH:18][C:17]([CH2:20][CH3:21])=[CH:16][C:12]=1[C:13]([OH:15])=[O:14])([CH3:8])[CH:5]([CH3:7])[CH3:6])(=[O:3])[NH2:2].C([O-])(=O)C.[Na+].BrBr>C(O)(=O)C>[CH2:20]([C:17]1[CH:18]=[N:19][C:11]([C:10]2[NH:2][C:1](=[O:3])[C:4]([CH:5]([CH3:7])[CH3:6])([CH3:8])[N:9]=2)=[C:12]([CH:16]=1)[C:13]([OH:15])=[O:14])[CH3:21]

Participants

5

Reactant 3

HCID 24408BromineHCID 517045Sodium AcetateHCID 146006872-{[(1-Carbamoyl-1,2-dimethylpropyl)amino]methyl}-5-ethylnicotinic acid

Product 1

HCID 54740ImazethapyrYield 51.2%

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

A mixture of 0.8 g of 2-{[(1-carbamoyl-1,2-dimethylpropyl)amino]methyl}-5-ethylnicotinic acid (2.7 mmol) and 0.56 g sodium acetate (6.8 mmol) in 10 mL acetic acid is warmed until homogeneous and cooled to room temperature. The solution is treated with 0.88 g bromine (5.45 mmol), and the reaction is stirred at 25° C. for 16 hours, then at 75° C. for three days. The reaction mixture is partitioned between CH2Cl2 and water, and the organic phase is dried and concentrated in vacuo. The residue is recrystallized from ethyl acetate-hexanes to afford 0.4 g of the title product having mp 172°-175° C.

Workup

  1. temperatureis warmed until homogeneous and
  2. waitat 75° C. for three days
  3. customThe reaction mixture is partitioned between CH2Cl2 and water
  4. customthe organic phase is dried
  5. concentrationconcentrated in vacuo
  6. customThe residue is recrystallized from ethyl acetate-hexanes

Sources & evidence

ORD record
ord-4ed438d58a1242759e32e094ecd38b43
Source dataset
uspto-grants-1992_04
Patent number
US05103009

Reaction notes

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