Sodium Hydroxide → HCID 66913476, compound
Reaction equation
[OH-].[Na+].[C:3]([C:11]1[CH:12]=[N:13][C:14]2[C:19]([C:20]=1[C:21]1[CH:22]=[C:23]([CH:42]=[CH:43][CH:44]=1)[O:24][CH2:25][C:26]1[CH:41]=[CH:40][C:29]([CH2:30][N:31]3[CH:35]=[CH:34][CH:33]=[C:32]3[C:36]([O:38]C)=[O:37])=[CH:28][CH:27]=1)=[CH:18][CH:17]=[CH:16][C:15]=2[C:45]([F:48])([F:47])[F:46])(=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>>[C:3]([C:11]1[CH:12]=[N:13][C:14]2[C:19]([C:20]=1[C:21]1[CH:22]=[C:23]([CH:42]=[CH:43][CH:44]=1)[O:24][CH2:25][C:26]1[CH:41]=[CH:40][C:29]([CH2:30][N:31]3[CH:35]=[CH:34][CH:33]=[C:32]3[C:36]([OH:38])=[O:37])=[CH:28][CH:27]=1)=[CH:18][CH:17]=[CH:16][C:15]=2[C:45]([F:47])([F:46])[F:48])(=[O:10])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1Participants
3
Procedure
Prepared by NaOH hydrolysis of methyl 1-[4-({3-[3-Benzoyl-8-(trifluoromethyl)quinolin-4-yl]phenoxy}methyl) benzyl]-1H-pyrrole-2-carboxylate; MS (ESI) m/z 607; MS (ESI) m/z 605.
Sources & evidence
- ORD record
- ord-b3424f677fc34bec8643cf45b43ac87f
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07576215B2
Reaction notes
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