N-苄氧羰基-L-亮氨酸 → N-[N-[(Phenylmethoxy)carbonyl]-L-leucyl]-L-norleucinol

HRID 73847

反应方程式

HRID 73847 反应方程式
[C:1]1([CH2:7][O:8][C:9]([NH:11][C@H:12]([C:17]([OH:19])=O)[CH2:13][CH:14]([CH3:16])[CH3:15])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:20][C@H:21]([CH2:26][OH:27])[CH2:22][CH2:23][CH2:24][CH3:25]>>[C:1]1([CH2:7][O:8][C:9]([NH:11][C@H:12]([C:17]([NH:20][C@H:21]([CH2:26][OH:27])[CH2:22][CH2:23][CH2:24][CH3:25])=[O:19])[CH2:13][CH:14]([CH3:15])[CH3:16])=[O:10])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

参与物

3

反应物 2

HCID 74840N-苄氧羰基-L-亮氨酸HCID 5494388L-己氨醇

产物 1

HCID 15168139N-[N-[(Phenylmethoxy)carbonyl]-L-leucyl]-L-norleucinol收率 58%

实验过程

N-[(phenylmethoxy)carbonyl]-L-leucine was used instead of 1-[[(phenylmethoxy)carbonyl]amino]cyclohexanecarboxylic acid, and L-norleucinol was used instead of L-valinol in the process according to Reference Example 178 to obtain 421 mg (58%) of the title compound.

来源与证据

ORD记录
ord-ac37e11a459a4ff08d4c2ee4c1c96d22
来源数据集
uspto-grants-2014_09
专利号
US08829209B2

关联笔记

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