Methanesulfonic Acid → HCID 86752152, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([CH3:12])(=[O:11])=[O:10])=[CH:5][C:4]=1[CH2:13][NH:14][C@H:15]1[CH:20]2[CH2:21][CH2:22][N:17]([CH2:18][CH2:19]2)[C@H:16]1[CH:23]([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.[CH3:36][S:37]([OH:40])(=[O:39])=[O:38]>CC(C)=O>[S:37]([OH:40])(=[O:39])(=[O:38])[CH3:36].[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([CH3:12])(=[O:11])=[O:10])=[CH:5][C:4]=1[CH2:13][NH:14][C@H:15]1[CH:20]2[CH2:19][CH2:18][N:17]([CH2:22][CH2:21]2)[C@H:16]1[CH:23]([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (2S,3S)-N-(2-methoxy-5-methylsulfonylphenyl)methyl-2-diphenylmethyl-1-azabicyclo[2.2.2]octan-3-amine (400 mg, 0.82 mmol) in acetone (10 mL) was added methanesulfonic acid (0.41 mmol, 39.2 mg). The precipitated white solid was filtered off to give the title compound (218 mg, 30.3%, 1st crop).
Workup
- filtrationThe precipitated white solid was filtered off
Sources & evidence
- ORD record
- ord-dc1de828b900414b9045f77505d1865d
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05721255
Reaction notes
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