Fumaric Acid → HCID 69831977, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[CH2:9][N:8]([C:15]([C@H:17]1[CH2:22][CH2:21][CH2:20][N:19]([CH2:23][CH2:24][C:25]([NH:27][C:28]3[CH:33]=[CH:32][C:31]4[O:34][CH2:35][O:36][C:30]=4[CH:29]=3)=[O:26])[CH2:18]1)=[O:16])[CH2:7][CH2:6]2.[C:37]([OH:44])(=[O:43])/[CH:38]=[CH:39]/[C:40]([OH:42])=[O:41]>C(O)C>[C:37]([OH:44])(=[O:43])/[CH:38]=[CH:39]/[C:40]([OH:42])=[O:41].[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[CH2:9][N:8]([C:15]([C@H:17]1[CH2:22][CH2:21][CH2:20][N:19]([CH2:23][CH2:24][C:25]([NH:27][C:28]3[CH:33]=[CH:32][C:31]4[O:34][CH2:35][O:36][C:30]=4[CH:29]=3)=[O:26])[CH2:18]1)=[O:16])[CH2:7][CH2:6]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a ethanol solution of 9.32 g of (±)-3-[(S)-3-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)piperidino]-N-(3,4-methylenedioxyphenyl)propanamide was added 2.07 g of fumaric acid, and the mixture was evaporated in vacuo. Thus, 9.38 g of (±)-3-[(S)-3-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)piperidino]-N-(3,4-methylenedioxyphenyl)propanamide fumarate was obtained as colorless crystals from ethanol/2-butanone.
Workup
- customthe mixture was evaporated in vacuo
Sources & evidence
- ORD record
- ord-02bd1b6e0ce44f0597e392876023d011
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06573279B1
Reaction notes
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