Hydrochloric Acid → HCID 66651457, compound
Reaction equation
[CH3:1][N:2]([CH3:30])[C:3]1([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH2:8][CH2:7][CH:6]([NH:9][C:10]([C:12]2[C:16]([CH3:17])=[N:15][N:14]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[N:13]=2)=[O:11])[CH2:5][CH2:4]1.Cl.[Cl:32][Si](C)(C)C.C(OC(C)C)(C)C>CC(=O)CC.C(OCC)(=O)C.O>[ClH:32].[CH3:30][N:2]([CH3:1])[C:3]1([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH2:8][CH2:7][CH:6]([NH:9][C:10]([C:12]2[C:16]([CH3:17])=[N:15][N:14]([C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)[N:13]=2)=[O:11])[CH2:5][CH2:4]1Participants
8
Procedure
As described for Example 120, 238 mg of the polar diastereoisomer of 5-methyl-2-phenyl-2H-[1,2,3]triazole-4-carboxylic acid (4-dimethylamino-4-phenylcyclohexyl)amide were also obtained, which, dissolved in 5 ml 2-butanone and 5 ml ethyl acetate, were converted into the corresponding hydrochloride by adding 10.6 μl water, 75 μl chlorotrimethylsilane and 10 ml diisopropylether (165 mg of white solid).
Workup
- customwere also obtained
Sources & evidence
- ORD record
- ord-a43ab801b3e2476abb33dfd4a17f4a44
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08093272B2
Reaction notes
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