Methanol → HCID 70077352, compound
Reaction equation
[OH-:1].[Na+].C([CH2:5][CH2:6][CH:7]1[CH:13]=[CH:12][N:11]([C:14](=[O:36])[C:15]2[CH:20]=[CH:19][C:18]([NH:21][C:22](=[O:35])[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=3[C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)=[CH:17][CH:16]=2)[C:10]2[CH:37]=[CH:38][CH:39]=[CH:40][C:9]=2[S:8]1)#N.[CH3:41][OH:42]>>[C:41]([CH2:5][CH2:6][CH:7]1[CH:13]=[CH:12][N:11]([C:14](=[O:36])[C:15]2[CH:16]=[CH:17][C:18]([NH:21][C:22](=[O:35])[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=3[C:29]3[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=3)=[CH:19][CH:20]=2)[C:10]2[CH:37]=[CH:38][CH:39]=[CH:40][C:9]=2[S:8]1)([OH:42])=[O:1]Participants
4
Procedure
A 6.6N NaOH solution (0.5 ml) was added to a mixture of Compound 30 as prepared in Example 17 (0.05 g, 0.096 mM) in methanol. The mixture was stirred at reflux overnight, cooled to room temperature and evaporated in vacuo. The residue was diluted with water and enough 6N HCl was added drop-wise to precipitate the product. The solid product was collected by filtration and dried. m/z (MH+)537
Workup
- temperatureat reflux overnight
- customevaporated in vacuo
- additionThe residue was diluted with water and enough 6N HCl
- additionwas added drop-wise
- customto precipitate the product
- filtrationThe solid product was collected by filtration
- customdried
Sources & evidence
- ORD record
- ord-1d5a6680d73e4dcf8ec6b230d4dfabf9
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06489321B1
Reaction notes
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