Hydrochloric Acid → 2-(3-(10,11-Dihydro-5h-dibenz[b,f]azepin-5-yl)-1-propyl)-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid hydrochloride
Reaction equation
C[O:2][C:3]([CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7][N:6]1[CH2:15][CH2:16][CH2:17][N:18]1[C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=2[CH2:22][CH2:21][C:20]2[CH:29]=[CH:30][CH:31]=[CH:32][C:19]1=2)=[O:4].C(O)C.[OH-].[Na+].[ClH:38]>O.O1CCCC1>[ClH:38].[CH:29]1[C:20]2[CH2:21][CH2:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=3[N:18]([CH2:17][CH2:16][CH2:15][N:6]3[CH:5]([C:3]([OH:4])=[O:2])[CH2:14][C:13]4[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=4)[CH2:7]3)[C:19]=2[CH:32]=[CH:31][CH:30]=1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of the above ester (0.80 g, 0.0019 mol), ethanol (5 ml), tetrahydrofuran (5 ml) and 4 N sodium hydroxide (4 ml) was stirred at room temperature for 22 h. Water (50 ml) and concentrated hydrochloric acid (2 ml) were added and the mixture was extracted with ethyl acetate (2×20 ml). The combined organic extracts were washed with brine (10 ml), dried (MgSO4) and concentrated in vacuo. This gave 0.8 g of a solid, which was triturated and washed with ethyl acetate (2×5 ml). Drying in vacuo, afforded 0.6 g (75%) of the title compound as a solid.
Workup
- extractionthe mixture was extracted with ethyl acetate (2×20 ml)
- washThe combined organic extracts were washed with brine (10 ml)
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customThis gave 0.8 g of a solid, which was triturated
- washwashed with ethyl acetate (2×5 ml)
- customDrying in vacuo
Sources & evidence
- ORD record
- ord-606e9d9075c14362b08a7944bcc43582
- Source dataset
- uspto-grants-2003_09
- Patent number
- US06613791B1
Reaction notes
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