Fumaric Acid → HCID 67170365, compound
Reaction equation
[N:1]1([C@H:7]2[CH2:11][CH2:10][N:9]([C:12]([C:14]3[CH:19]=[CH:18][C:17]([N:20]4[C:24]5[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=5[N:22]=[CH:21]4)=[CH:16][CH:15]=3)=O)[CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:29]([OH:36])(=[O:35])/[CH:30]=[CH:31]/[C:32]([OH:34])=[O:33]>>[C:29]([OH:36])(=[O:35])/[CH:30]=[CH:31]/[C:32]([OH:34])=[O:33].[N:1]1([C@H:7]2[CH2:11][CH2:10][N:9]([CH2:12][C:14]3[CH:15]=[CH:16][C:17]([N:20]4[C:24]5[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=5[N:22]=[CH:21]4)=[CH:18][CH:19]=3)[CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
3
Procedure
Using essentially the same procedure described in Example 14 and employing 1-(4-{[(3S)-3-piperidin-1-ylpyrrolidin-1-yl]carbonyl}phenyl)-1H-benzimidazole as starting material and fumaric acid, the title compound was obtained and identified by NMR and mass spectral analyses. MS [361.2 m/e (M+H)].
Sources & evidence
- ORD record
- ord-1dee098a83f146828203c0d8f3c12918
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07935719B2
Reaction notes
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