Hydrochloric Acid → HCID 21193249, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][C:11]([C:18](=[O:26])[C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([CH3:25])[CH:20]=2)([C:14]([O:16][CH3:17])=[O:15])[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:27]>C(OCC)(=O)C>[ClH:27].[CH3:25][C:21]1[CH:20]=[C:19]([CH:24]=[CH:23][CH:22]=1)[C:18]([C:11]1([C:14]([O:16][CH3:17])=[O:15])[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]1)=[O:26]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of methyl N-tert-butoxycarbonyl-4-(3-methyl-benzoyl)piperidine-4-carboxylate (77 mg) in ethyl acetate (10 mL) at 0° C. was saturated with hydrogen chloride gas. The resultant solution was stirred at 0° C. for 2.5 h. The product solution was concentrated under vacuum to provide the title compound.
Workup
- customat 0° C.
- concentrationThe product solution was concentrated under vacuum
Sources & evidence
- ORD record
- ord-491de4bf7fb2437d90b018f2b65a6bc9
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06248756B1
Reaction notes
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