(R)-2-(BOC-氨基)-3-苯基丙胺 → N,N-bis[(2R)-2-(tert-butoxycarbonylamino)-3-phenylpropyl]amine

反应方程式

[NH2:1][CH2:2][C@H:3]([NH:11][C:12](=[O:18])[O:13][C:14]([CH3:17])([CH3:16])[CH3:15])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[C:19]([O:23][C:24]([N:26]1[CH2:28][C@H:27]1[CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)=[O:25])([CH3:22])([CH3:21])[CH3:20]>>[C:14]([O:13][C:12]([NH:11][C@H:3]([CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[CH2:2][NH:1][CH2:28][C@H:27]([NH:26][C:24]([O:23][C:19]([CH3:20])([CH3:22])[CH3:21])=[O:25])[CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)=[O:18])([CH3:15])([CH3:17])[CH3:16]

参与物

反应物 2

HCID 42645993(R)-2-(BOC-氨基)-3-苯基丙胺

HCID 60204744(2R)-N-tert-butoxycarbonyl-2-phenylmethylaziridine

产物 1

HCID 60204745N,N-bis[(2R)-2-(tert-butoxycarbonylamino)-3-phenylpropyl]amine

实验过程

The product from Example 70C and the product from Example 70A were processed as described in Example 1D to provide the title compound.

来源与证据

ORD记录: ord-190144e5a7734fafaeb7056df09d39ef
来源数据集: uspto-grants-2014_06
DOI: 10.6084/m9.figshare.5104873.v1
专利号: US08741938B2

反应笔记

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