(2S,3S)-3-Amino-1-tert-butoxycarbonyl-2-phenylpiperidine → (2S,3S)-1-tert-Butoxycarbonyl-3-(5-(1-cyano-1-methylethyl)-2-isopropoxybenzyl)amino-2-phenylpiperidine

HRID 481514Notes

Reaction equation

HRID 481514 reaction equation
[C:1]([C:3]([C:6]1[CH:7]=[CH:8][C:9]([O:14][CH:15]([CH3:17])[CH3:16])=[C:10]([CH:13]=1)[CH:11]=O)([CH3:5])[CH3:4])#[N:2].[NH2:18][C@H:19]1[CH2:24][CH2:23][CH2:22][N:21]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[C@H:20]1[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1.C(OC(N1CCC[C@H](NCC2C=C(C(C#N)C)C=CC=2OC)[C@@H]1C1C=CC=CC=1)=O)(C)(C)C>>[C:28]([O:27][C:25]([N:21]1[CH2:22][CH2:23][CH2:24][C@H:19]([NH:18][CH2:11][C:10]2[CH:13]=[C:6]([C:3]([C:1]#[N:2])([CH3:5])[CH3:4])[CH:7]=[CH:8][C:9]=2[O:14][CH:15]([CH3:17])[CH3:16])[C@@H:20]1[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)=[O:26])([CH3:31])([CH3:29])[CH3:30]

Participants

4

Procedure

This compound was prepared from Compound 41 and Compound 17 in the same manner of Compound 18.

Sources & evidence

ORD record
ord-ac594c07468740e494a26fa03474a20f
Source dataset
uspto-grants-1998_08
Patent number
US05789423

Reaction notes

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