Ethanol → HCID 58345798, compound
Reaction equation
[CH2:1]([N:4]([CH2:37][CH2:38][CH3:39])[CH2:5][CH2:6][CH2:7][CH2:8][N:9]([CH2:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][N:23]([CH2:31][C:32]2[NH:33][CH:34]=[CH:35][N:36]=2)[CH2:24][C:25]2[N:26]([CH3:30])[CH:27]=[CH:28][N:29]=2)=[CH:18][CH:17]=1)[CH2:10][CH2:11][C:12]([OH:14])=[O:13])[CH2:2][CH3:3].[CH2:40](O)[CH3:41]>>[CH2:40]([O:13][C:12](=[O:14])[CH2:11][CH2:10][N:9]([CH2:8][CH2:7][CH2:6][CH2:5][N:4]([CH2:1][CH2:2][CH3:3])[CH2:37][CH2:38][CH3:39])[CH2:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][N:23]([CH2:31][C:32]2[NH:33][CH:34]=[CH:35][N:36]=2)[CH2:24][C:25]2[N:26]([CH3:30])[CH:27]=[CH:28][N:29]=2)=[CH:18][CH:17]=1)[CH3:41]Participants
3
Procedure
The compound (135.4 mg) obtained in Example 51-1 was suspended in ethanol (13.5 ml) and the whole was refluxed under heating for 16 hours. After completion of the reaction, the solvent was distilled off. The resultant was added with saturated sodium hydrogen carbonate aqueous solution and the whole was subjected to extraction with chloroform. The resultant was dried with magnesium sulfate and the solvent was distilled off, thereby obtaining the subject compound (127.0 mg) as a colorless oily substance.
Workup
- temperaturethe whole was refluxed
- temperatureunder heating for 16 hours
- customAfter completion of the reaction
- distillationthe solvent was distilled off
- additionThe resultant was added with saturated sodium hydrogen carbonate aqueous solution
- extractionthe whole was subjected to extraction with chloroform
- dry with materialThe resultant was dried with magnesium sulfate
- distillationthe solvent was distilled off
Sources & evidence
- ORD record
- ord-059d5ad94a5f48d9a75cc726fe23fa63
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07932281B2
Reaction notes
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