Sodium Hydroxide → HCID 58730629, compound
Reaction equation
C[O:2][C:3](=[O:42])[CH2:4][CH:5]1[C:14]2[C:9](=[C:10]([F:15])[CH:11]=[CH:12][CH:13]=2)[N:8]=[C:7]([C:16]2[CH:21]=[CH:20][C:19]([C:22]3[CH:27]=[CH:26][CH:25]=[C:24]([O:28][CH3:29])[CH:23]=3)=[CH:18][CH:17]=2)[N:6]1[C:30]1[CH:35]=[C:34]([C:36]([F:39])([F:38])[F:37])[CH:33]=[CH:32][C:31]=1[O:40][CH3:41].[OH-].[Na+]>O1CCOCC1>[CH3:29][O:28][C:24]1[CH:23]=[C:22]([C:19]2[CH:20]=[CH:21][C:16]([C:7]3[N:6]([C:30]4[CH:35]=[C:34]([C:36]([F:39])([F:38])[F:37])[CH:33]=[CH:32][C:31]=4[O:40][CH3:41])[CH:5]([CH2:4][C:3]([OH:42])=[O:2])[C:14]4[C:9](=[C:10]([F:15])[CH:11]=[CH:12][CH:13]=4)[N:8]=3)=[CH:17][CH:18]=2)[CH:27]=[CH:26][CH:25]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Starting from 459 mg (0.79 mmol) of the ester from Example 22A, reaction in analogy to general method [E] with 95.2 mg (2.38 mmol) of sodium hydroxide in 54 ml of dioxane results in 383 mg (86% of theory) of the target compound.
Workup
- customresults in 383 mg (86% of theory) of the target compound
Sources & evidence
- ORD record
- ord-267064bdd3df4e9a9f44fe8181ef61a5
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07709491B2
Reaction notes
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