Tert-butyl 3-amino-2-phenylpiperidine-1-carboxylate → (2s,3s)-1-Tert-butoxycarbonyl-3-(2,4-dimethoxy-5-(2,2,2-trifluoroethyl)benzyl)amino-2-phenylpiperidine

HRID 1634362Notes

Reaction equation

HRID 1634362 reaction equation
[NH2:1][CH:2]1[CH2:7][CH2:6][CH2:5][N:4]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH:3]1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[CH3:21][O:22][C:23]1[CH:30]=[C:29]([O:31][CH3:32])[C:28]([CH2:33][C:34]([F:37])([F:36])[F:35])=[CH:27][C:24]=1[CH:25]=O>>[C:11]([O:10][C:8]([N:4]1[CH2:5][CH2:6][CH2:7][C@H:2]([NH:1][CH2:25][C:24]2[CH:27]=[C:28]([CH2:33][C:34]([F:35])([F:36])[F:37])[C:29]([O:31][CH3:32])=[CH:30][C:23]=2[O:22][CH3:21])[C@@H:3]1[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)=[O:9])([CH3:14])([CH3:13])[CH3:12]

Participants

3

Reactant 2

HCID 10214733Tert-butyl 3-amino-2-phenylpiperidine-1-carboxylateHCID 186776582,4-Dimethoxy-5-(2,2,2-trifluoroethyl)benzaldehyde

Product 1

HCID 57285369(2s,3s)-1-Tert-butoxycarbonyl-3-(2,4-dimethoxy-5-(2,2,2-trifluoroethyl)benzyl)amino-2-phenylpiperidine

Procedure

This compound was prepared from Compound 12 and Compound 85 in the same manner of Compound 13.

Sources & evidence

ORD record
ord-259b8b22b6b6455da95c57c364de5b8a
Source dataset
uspto-grants-2003_01
Patent number
US06506775B1

Reaction notes

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