Sodium Hydroxide → HCID 9850580, compound
Reaction equation
C[O:2][C:3](=[O:41])[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][C:25]([F:28])=[CH:24][CH:23]=3)=[CH:18][CH:17]=2)[N:6]1[C:29]1[CH:34]=[C:33]([C:35]([F:38])([F:37])[F:36])[CH:32]=[CH:31][C:30]=1[O:39][CH3:40].[OH-].[Na+]>O1CCOCC1>[F:28][C:25]1[CH:26]=[CH:27][C:22]([C:19]2[CH:18]=[CH:17][C:16]([C:7]3[N:6]([C:29]4[CH:34]=[C:33]([C:35]([F:37])([F:38])[F:36])[CH:32]=[CH:31][C:30]=4[O:39][CH3:40])[CH:5]([CH2:4][C:3]([OH:41])=[O:2])[C:14]4[C:9](=[C:10]([F:15])[CH:11]=[CH:12][CH:13]=4)[N:8]=3)=[CH:21][CH:20]=2)=[CH:23][CH:24]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Starting from 38.90 (0.07 mmol) of the ester from Example 20A, reaction in analogy to general method [E] with 8.24 mg (0.21 mmol) of sodium hydroxide in 10 ml of dioxane results in 29 mg (76% of theory) of the target compound.
Workup
- customresults in 29 mg (76% of theory) of the target compound
Sources & evidence
- ORD record
- ord-2143ff12755a40b987e661ecafd14087
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07709491B2
Reaction notes
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