Methanol → HCID 59186993, compound
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]=1Participants
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
- temperaturethe mixture is heated
- temperatureunder reflux overnight
- temperatureAfter cooling
- customthe precipitate formed
- filtrationis filtered off with suction
- washwashed with methanol
- customdried
Sources & evidence
- ORD record
- ord-69e6e206a5af4db69f83945f268ec4c1
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252817B2
Reaction notes
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