Reaction equation
[CH2:1]([N:3]1[C:12]2[C:7](=[CH:8][C:9]([CH3:26])=[C:10]([C:13]3[CH:14]=[C:15]([CH:18]=[CH:19][C:20]=3[O:21][C:22]([F:25])([F:24])[F:23])C=O)[CH:11]=2)[C:6]([CH3:28])([CH3:27])[CH2:5][C:4]1=[O:29])[CH3:2].[CH2:30]([CH:32](P(O)(O)=O)/[C:33](/CC)=[C:34](\CC)/[C:35]([O-:37])=[O:36])C>>[CH2:1]([N:3]1[C:12]2[C:7](=[CH:8][C:9]([CH3:26])=[C:10]([C:13]3[CH:14]=[C:15]([CH:30]=[CH:32][CH:33]=[CH:34][C:35]([OH:37])=[O:36])[CH:18]=[CH:19][C:20]=3[O:21][C:22]([F:24])([F:25])[F:23])[CH:11]=2)[C:6]([CH3:28])([CH3:27])[CH2:5][C:4]1=[O:29])[CH3:2]Participants
3
Reactant 2
Product 1
Procedure
Compound 24 was prepared from Compound 2A using procedures similar to those described for Example 20B and 20C, except using triethyl-4-phosphonocrotonate in step 20B. MS (electrospray): mass calculated for C26H26F3NO4, 473.18; m/z found 474.2 [M+H]+.
Sources & evidence
- ORD record
- ord-90df589969f8493183119a984d2796a3
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07638533B2
Linked notes
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