HCID 87734433, compound → HCID 10339980, compound
Reaction equation
C([O:5][C:6](=[O:51])[CH2:7][CH:8]([C:34](=[O:50])[NH:35][CH2:36][CH2:37][C:38]1[CH:43]=[CH:42][C:41]([C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)=[CH:40][CH:39]=1)[CH2:9][CH2:10][C:11](=[O:33])[NH:12][O:13]C(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)(C)(C)C.ONC(CC(C(=O)NCCC1C2C(=CC=CC=2)NC=1)CC(O)=O)=O>>[C:41]1([C:44]2[CH:45]=[CH:46][CH:47]=[CH:48][CH:49]=2)[CH:42]=[CH:43][C:38]([CH2:37][CH2:36][NH:35][C:34]([CH:8]([CH2:9][CH2:10][C:11](=[O:33])[NH:12][OH:13])[CH2:7][C:6]([OH:51])=[O:5])=[O:50])=[CH:39][CH:40]=1Participants
3
Procedure
This compound was prepared by deprotection of the compound of Example 151, as previously described for the compound of Example 128.
Sources & evidence
- ORD record
- ord-a66469bbac9849fca6b3ccb054274400
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365091B2
Reaction notes
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