Trifluoroacetic acid → HCID 117856453, compound
Reaction equation
[Cl-:1].C(OC([NH:9][CH:10]1[CH2:15][CH2:14][CH2:13][N+:12]([CH2:31][CH2:32][CH2:33][C:34]2[CH:39]=[CH:38][C:37]([O:40][CH2:41][C:42]([O:44][CH3:45])=[O:43])=[CH:36][CH:35]=2)([CH2:16][CH2:17][CH2:18][C:19]2[CH:24]=[CH:23][C:22]([O:25][CH2:26][C:27]([O:29][CH3:30])=[O:28])=[CH:21][CH:20]=2)[CH2:11]1)=O)(C)(C)C.FC(F)(F)C(O)=O>ClCCl>[ClH:1].[Cl-:1].[NH2:9][CH:10]1[CH2:15][CH2:14][CH2:13][N+:12]([CH2:31][CH2:32][CH2:33][C:34]2[CH:39]=[CH:38][C:37]([O:40][CH2:41][C:42]([O:44][CH3:45])=[O:43])=[CH:36][CH:35]=2)([CH2:16][CH2:17][CH2:18][C:19]2[CH:20]=[CH:21][C:22]([O:25][CH2:26][C:27]([O:29][CH3:30])=[O:28])=[CH:23][CH:24]=2)[CH2:11]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-tert-Butoxycarbonylamino-1,1-bis-[3-(4-methoxycarbonylmethoxy-phenyl)-propyl]-piperidinium chloride (707 mg, 1.09 mmol) is dissolved in dichloromethane (1 ml) and trifluoroacetic acid (1 ml) and stirred at room temperature overnight. The mixture is evaporated, dissolved in acetonitrile and 1 M HCl (5 ml) and evaporated again. LC (method L): tR=0.95 min; Mass spectrum (ESI+): m/z=513 [M]+.
Workup
- customThe mixture is evaporated
- dissolutiondissolved in acetonitrile
- custom1 M HCl (5 ml) and evaporated again
Sources & evidence
- ORD record
- ord-b568d82401dd4ea9ad9ae02b82c72da8
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09096548B2
Reaction notes
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