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(2S,3S)-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 2269285
Notes
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Reaction equation

HRID 2269285 reaction equation
[NH2:1][C@H:2]1[CH2:7][CH2:6][CH2:5][N:4]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[C@H: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(OC(N1CCC[C@H](NCC2C=C(C(C(F)(F)F)C(F)(F)F)C=CC=2OC)[C@@H]1C1C=CC=CC=1)=O)(C)(C)C>>[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]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 11311934(2S,3S)-tert-Butyl 3-amino-2-phenylpiperidine-1-carboxylateHCID 15549735(2S, 3S)-1-tert-Butoxycarbonyl-2-phenyl-3-(5-(2,2,2-trifluoro-1-(trifluoromethyl)ethyl)-2-methoxybenzyl)aminopiperidineHCID 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-c6b33d89d4e44640b3658ebf9fe46851
Source dataset
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06329396B1

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes