Sodium Hydroxide → (R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid sodium salt hydrate
Reaction equation
[Cl:1][C:2]1[C:10]2[CH:9]=[C:8]([O:11][CH2:12][C:13]3[CH:18]=[CH:17][C:16]([O:19][CH:20]([CH3:22])[CH3:21])=[C:15]([C:23]([F:26])([F:25])[F:24])[CH:14]=3)[CH:7]=[CH:6][C:5]=2[N:4]2[CH2:27][CH2:28][C@H:29]([CH2:30][C:31]([OH:33])=[O:32])[C:3]=12.[OH-].[Na+:35]>CC(O)C>[OH2:11].[Na+:35].[Cl:1][C:2]1[C:10]2[CH:9]=[C:8]([O:11][CH2:12][C:13]3[CH:18]=[CH:17][C:16]([O:19][CH:20]([CH3:22])[CH3:21])=[C:15]([C:23]([F:24])([F:25])[F:26])[CH:14]=3)[CH:7]=[CH:6][C:5]=2[N:4]2[CH2:27][CH2:28][C@H:29]([CH2:30][C:31]([O-:33])=[O:32])[C:3]=12Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
(R)-2-(9-Chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid (20 mg) was dissolved in IPA (0.5 mL) with heating, and 2.0 M NaOH (21 uL) was added. The solution was allowed to cool to room temperature and stir for 24 h. The resultant solids that had formed were collected after decanting off the IPA.
Workup
- temperaturewith heating
- customThe resultant solids that had formed
- customwere collected
- customafter decanting off the IPA
Sources & evidence
- ORD record
- ord-a22f14d541e54a129101dd77f6e21fdb
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09085581B2
Reaction notes
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