Hydrazine hydrate (1:1) → HCID 11162571, compound

HRID 2188025Notes

Reaction equation

HRID 2188025 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

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

  1. customThe solvent was removed in vacuo
  2. extractionthe solid residue was extracted with refluxing diethyl ether
  3. 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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