5-Iodoisatin → HCID 178521413, compound

HRID 642055Notes

Reaction equation

HRID 642055 reaction equation
[I:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2=O.[I:13][C:14]1[CH:25]=[CH:24][C:17]([O:18][CH2:19][C:20]([NH:22][NH2:23])=[O:21])=[CH:16][CH:15]=1>C(O)(=O)C>[I:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2=[N:23][NH:22][C:20](=[O:21])[CH2:19][O:18][C:17]1[CH:24]=[CH:25][C:14]([I:13])=[CH:15][CH:16]=1

Participants

4

Reactant 2

HCID 886955-IodoisatinHCID 7815502-(4-Iodophenoxy)acetohydrazide

Product 1

HCID 178521413HCID 178521413, compoundYield 79%

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Conditions

Temperature
100 °C

Procedure

Following the general method as outlined in Example 1, into a suspension of 5-iodo-1H-indole-2,3-dione in acetic acid was added 2-(4-iodophenoxy)acetohydrazide. After stirring at 100° C., the reaction mixture was cooled to rt and a yellow solid precipitated out. Filtration on a fritté, washing with AcOH, water and drying under vacuo at 60° C. overnight gave 173 mg of the title compound (79%) as a yellow solid in 96.4% purity by HPLC (Rt: 6.41, gradient of 10 min, MaxPlot detection between 230 and 400 nm).

Workup

  1. temperaturethe reaction mixture was cooled to rt
  2. customa yellow solid precipitated out
  3. filtrationFiltration on a fritté
  4. washwashing with AcOH, water
  5. customdrying under vacuo at 60° C. overnight

Sources & evidence

ORD record
ord-a53ad26fa89e4f18b9bd49fb2fc0dba3
Source dataset
uspto-grants-2010_04
Patent number
US07696231B2

Reaction notes

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