Hydrazine hydrate (1:1) → HCID 11162571, compound
Reaction equation
[CH2:1]([O:3][C:4]1([O:30][CH2:31][CH3:32])[CH2:9][CH2:8][N:7]([C@H:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH3:11])[C@@H:6]([CH2:18][N:19]2C(=O)C3=CC=CC=C3C2=O)[CH2:5]1)[CH3:2].O.NN>C(O)C>[CH2:31]([O:30][C:4]1([O:3][CH2:1][CH3:2])[CH2:9][CH2:8][N:7]([C@H:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH3:11])[C@@H:6]([CH2:18][NH2:19])[CH2:5]1)[CH3:32]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4,4-diethoxy-1-((S)-1-phenyl-ethyl)-(R)-2-phthalimidomethyl-piperidine (5.25 g, 12.0 mmol) and hydrazine hydrate (2.92 ml, 60 mmol) was stirred overnight in ethanol (100 ml) at room temperature. The solvent was removed in vacuo and the solid residue was extracted with refluxing diethyl ether. The diethyl ether fractions were combined and evaporated in vacuo, which afforded 3.94 g (94%) of 4,4-diethoxy-1-((S)-1-phenyl-ethyl)-(R)-2-aminomethyl-piperidine as an oil.
Workup
- customThe solvent was removed in vacuo
- extractionthe solid residue was extracted with refluxing diethyl ether
- customevaporated in vacuo, which
Sources & evidence
- ORD record
- ord-4a7a37a25a5045c0813d0a4c5bbfa5c6
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06410556B1
Reaction notes
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