Methanol → HCID 58868898, compound
Reaction equation
[CH2:1]([O:8][C:9]1[CH:27]=[CH:26][C:25]2=[CH:28][C:10]=1[CH2:11][C@H:12]([NH:65][C:66]([O:68][CH2:69][C:70]1[CH:75]=[CH:74][CH:73]=[CH:72][CH:71]=1)=[O:67])[C:13](=[O:64])[NH:14][C@@H:15]([CH2:42][C@@H:43]([O:56][Si:57]([C:60]([CH3:63])([CH3:62])[CH3:61])([CH3:59])[CH3:58])[CH2:44][NH:45][C:46]([O:48][CH2:49][C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=1)=[O:47])[C:16](=[O:41])[NH:17][C@H:18]([C:31]([O:33]CC1C=CC=CC=1)=[O:32])[CH2:19][C:20]1[CH:29]=[C:24]2[CH:23]=[CH:22][C:21]=1[Cl:30])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.CO.[OH-].[Li+]>C1COCC1>[CH2:1]([O:8][C:9]1[CH:27]=[CH:26][C:25]2=[CH:28][C:10]=1[CH2:11][C@H:12]([NH:65][C:66]([O:68][CH2:69][C:70]1[CH:71]=[CH:72][CH:73]=[CH:74][CH:75]=1)=[O:67])[C:13](=[O:64])[NH:14][C@@H:15]([CH2:42][C@@H:43]([O:56][Si:57]([C:60]([CH3:63])([CH3:62])[CH3:61])([CH3:59])[CH3:58])[CH2:44][NH:45][C:46]([O:48][CH2:49][C:50]1[CH:51]=[CH:52][CH:53]=[CH:54][CH:55]=1)=[O:47])[C:16](=[O:41])[NH:17][C@H:18]([C:31]([OH:33])=[O:32])[CH2:19][C:20]1[CH:29]=[C:24]2[CH:23]=[CH:22][C:21]=1[Cl:30])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
220 mg (0.21 mmol) of the compound from Example 25C are dissolved in 11 ml of THF, and 3 ml each of water and methanol are added. After the addition of 10.2 mg (0.43 mmol) of lithium hydroxide the mixture is stirred at RT for 24 h. The reaction solution is then concentrated in vacuo, and the crude product is dried under high vacuum.
Workup
- concentrationThe reaction solution is then concentrated in vacuo
- dry with materialthe crude product is dried under high vacuum
Sources & evidence
- ORD record
- ord-c10cc867c8a7430f8b305ce6ae8145e6
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07655643B2
Reaction notes
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