Methanol → HCID 59186993, compound

HRID 889314Notes

Reaction equation

HRID 889314 reaction equation
[O:1]=[C:2]1[N:6]([C:7]2[CH:8]=[C:9]([CH:13]=[CH:14][N:15]=2)[C:10]([OH:12])=[O:11])[NH:5][CH:4]=[C:3]1[C:16]1[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=1.S(=O)(=O)(O)O.[CH3:27]O>>[CH3:27][O:11][C:10](=[O:12])[C:9]1[CH:13]=[CH:14][N:15]=[C:7]([N:6]2[C:2](=[O:1])[C:3]([C:16]3[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=3)=[CH:4][NH:5]2)[CH:8]=1

Participants

4

Procedure

150 mg (531 μmol) of the compound from Example 41 are dissolved in 20 ml methanol, 1 ml concentrated sulfuric acid are added and the mixture is heated under reflux overnight. After cooling, the precipitate formed is filtered off with suction, washed with methanol and dried.

Workup

  1. temperaturethe mixture is heated
  2. temperatureunder reflux overnight
  3. temperatureAfter cooling
  4. customthe precipitate formed
  5. filtrationis filtered off with suction
  6. washwashed with methanol
  7. customdried

Sources & evidence

ORD record
ord-69e6e206a5af4db69f83945f268ec4c1
Source dataset
uspto-grants-2012_08
Patent number
US08252817B2

Reaction notes

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