Water → 6-Methoxy-5-methyl-2-nitro-3-pyridinamine

HRID 505381Notes

Reaction equation

HRID 505381 reaction equation
[CH3:1][O:2][C:3]1[N:8]=[C:7]([N+:9]([O-:11])=[O:10])[C:6]([NH:12]C(=O)C)=[CH:5][C:4]=1[CH3:16].[OH-].[Na+].O>CO>[CH3:1][O:2][C:3]1[N:8]=[C:7]([N+:9]([O-:11])=[O:10])[C:6]([NH2:12])=[CH:5][C:4]=1[CH3:16]

Participants

5

Procedure

The crude product (1.93 g) of N-(6-methoxy-5-methyl-2-nitro-3-pyridinyl) acetamide was dissolved in methanol (36 ml), 5N sodium hydroxide solution (6 ml) was added, and the reaction mixture was stirred for 15 minutes at room temperature. After water was added to the reaction solution, it was extracted with ethyl acetate and dried over magnesium sulfate, and the solvent was evaporated, thereby yielding the title compound (1.06 g, 5.79 mmol) as a yellow solid.

Workup

  1. extractionwas extracted with ethyl acetate
  2. dry with materialdried over magnesium sulfate
  3. customthe solvent was evaporated

Sources & evidence

ORD record
ord-7e8cb2b8bc3f4da4a4c933dcf9bf1f6b
Source dataset
uspto-grants-2010_08
Patent number
US07781452B2

Reaction notes

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