(2S,3S)-3-(2-methoxy-5-(1,1-dimethyl-2-propynyl)benzyl)amino-2-phenylpiperidine → (2S,3S)-3-(2-methoxy-5-(1,1-dimethyl-2-propynyl)benzyl)amino-2-phenylpiperidine Dihydrochloride

HRID 481503Notes

Reaction equation

HRID 481503 reaction equation
[CH3:1][O:2][C:3]1[CH:22]=[CH:21][C:20]([C:23]([CH3:27])([CH3:26])[C:24]#[CH:25])=[CH:19][C:4]=1[CH2:5][NH:6][C@H:7]1[CH2:12][CH2:11][CH2:10][NH:9][C@H:8]1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[ClH:28].Cl.C(C(C1C=CC(OC)=C(C=1)CN[C@H]1CCCN[C@H]1C1C=CC=CC=1)C)#N>>[ClH:28].[ClH:28].[CH3:1][O:2][C:3]1[CH:22]=[CH:21][C:20]([C:23]([CH3:27])([CH3:26])[C:24]#[CH:25])=[CH:19][C:4]=1[CH2:5][NH:6][C@H:7]1[CH2:12][CH2:11][CH2:10][NH:9][C@H:8]1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Participants

3

Reactant 2

HCID 57071301(2S,3S)-3-(2-methoxy-5-(1,1-dimethyl-2-propynyl)benzyl)amino-2-phenylpiperidineHCID 70137377(2S,3S)-3-(5-(1-cyanoethyl)-2-methoxybenzyl)amino-2-phenylpiperidine Dihydrochloride

Product 1

HCID 86752970(2S,3S)-3-(2-methoxy-5-(1,1-dimethyl-2-propynyl)benzyl)amino-2-phenylpiperidine Dihydrochloride

Procedure

This compound was prepared from Compound 24 in the same manner of Compound 20.

Sources & evidence

ORD record
ord-d744c2a722414c9c9831d5f8a82308aa
Source dataset
uspto-grants-1998_08
Patent number
US05789423

Reaction notes

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