Hydrochloric Acid → HCID 10027772, compound
Reaction equation
[ClH:1].[NH:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]([C:11]2[CH2:12][CH2:13][N:14]([CH:17]3[CH2:22][CH2:21][C:20]([N:29]([CH3:31])[CH3:30])([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[CH2:19][CH2:18]3)[CH2:15][CH:16]=2)=[CH:3]1.[Cl:32][Si](C)(C)C>CC(CC)=O>[ClH:32].[ClH:1].[NH:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]([C:11]2[CH2:12][CH2:13][N:14]([CH:17]3[CH2:18][CH2:19][C:20]([N:29]([CH3:31])[CH3:30])([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[CH2:21][CH2:22]3)[CH2:15][CH:16]=2)=[CH:3]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To prepare the hydrochloride the diastereoisomer mixture of {4-[4-(1H-indol-3-yl)-3,6-dihydro-2H-pyridine-1-yl]-1-phenylcyclohexyl}-dimethylamine (320 mg, 0.8 mmole) was dissolved in ethyl methyl ketone (5 ml) and chlorotrimethylsilane (255 μl, 2.0 mmole) was added. The solid thereby formed was filtered off and dried. The hydrochloride was thereby obtained in a yield of 378 mg (100%) as a colourless solid (Example 56) with an m.p. of 188°-191° C.
Workup
- customThe solid thereby formed
- filtrationwas filtered off
- customdried
Sources & evidence
- ORD record
- ord-d9338f3e48e847c8a11464ad29df5cee
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07759385B2
Reaction notes
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