(2S,3S)-3-Amino-1-tert-butoxycarbonyl-2-phenylpiperidine → (2S,3S)-1-tert-Butoxycarbonyl-3-(5-cyanomethyl-2-methoxybenzyl)amino-2-phenylpiperidine

HRID 481537Notes

Reaction equation

HRID 481537 reaction equation
N[C@H]1CCCN(C(OC(C)(C)C)=O)[C@H]1C1C=CC=CC=1.[C:21]([O:25][C:26]([N:28]1[CH2:33][CH2:32][CH2:31][C@H:30]([NH:34][CH2:35][C:36]2[CH:41]=[C:40]([CH:42]([C:44]#[N:45])C)[CH:39]=[CH:38][C:37]=2[O:46][CH3:47])[C@@H:29]1[C:48]1[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=1)=[O:27])([CH3:24])([CH3:23])[CH3:22]>>[C:21]([O:25][C:26]([N:28]1[CH2:33][CH2:32][CH2:31][C@H:30]([NH:34][CH2:35][C:36]2[CH:41]=[C:40]([CH2:42][C:44]#[N:45])[CH:39]=[CH:38][C:37]=2[O:46][CH3:47])[C@@H:29]1[C:48]1[CH:49]=[CH:50][CH:51]=[CH:52][CH:53]=1)=[O:27])([CH3:24])([CH3:22])[CH3:23]

Participants

3

Reactant 2

HCID 11311934(2S,3S)-3-Amino-1-tert-butoxycarbonyl-2-phenylpiperidineHCID 57028229(2S,3S)-1-tert-Butoxycarbonyl-3-(5-(1-cyanoethyl)-2-methoxybenzyl)amino-2-phenylpiperidine

Product 1

HCID 57083866(2S,3S)-1-tert-Butoxycarbonyl-3-(5-cyanomethyl-2-methoxybenzyl)amino-2-phenylpiperidine

Procedure

This compound was prepared from Compound 71 and Compound 17 in the same manner of Compound 18.

Sources & evidence

ORD record
ord-413640a393864ecbbd28c9aead38d1af
Source dataset
uspto-grants-1998_08
Patent number
US05789423

Reaction notes

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