2-methylsulfanyl-5-nitropyrimidine → 5-Pyrimidinamine, 2-(methylthio)- (9CI)

HRID 2387288Notes

Reaction equation

HRID 2387288 reaction equation
[CH3:1][S:2][C:3]1[N:8]=[CH:7][C:6]([N+:9]([O-])=O)=[CH:5][N:4]=1>C(O)C.C(O)(=O)C.C(OCC)(=O)C.[Fe]>[CH3:1][S:2][C:3]1[N:8]=[CH:7][C:6]([NH2:9])=[CH:5][N:4]=1

Participants

6

Conditions

Temperature
80 °C

Procedure

A solution of 5 g (29.2 mmol) of 2-methylsulfanyl-5-nitropyrimidine in 200 mL of absolute ethanol and 120 mL of glacial acetic acid was added 16.31 g (292 mmol) of iron powder and the mixture was heated in an oil bath maintained at 80° C. for 2 hours. The reaction was diluted with 250 mL of ethyl acetate and filtered through CELITE® filter aid. The filtrate was washed with two portions of 100 mL of water, and the pH of the organic layer was adjusted by adding saturated aqueous sodium carbonate solution until the pH was 8. The organic layer washed with brine, dried over sodium sulfate, and concentrated in vacuo to afford 2.1 g (51%) of 2-methylsulfanylpyrimidin-5-ylamine.

Workup

  1. temperaturethe mixture was heated in an oil bath
  2. filtrationfiltered through CELITE®
  3. filtrationfilter aid
  4. washThe filtrate was washed with two portions of 100 mL of water
  5. additionby adding saturated aqueous sodium carbonate solution until the pH was 8
  6. washThe organic layer washed with brine
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-5177716697f34f94b9df12948837c552
Source dataset
uspto-grants-2012_09
Patent number
US08268859B2

Reaction notes

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