HRID272071

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7284

2-Methylbutanal

C5H10O

结构：O=C(CCCCCNC(=O)CC(c1ccccc1)(c1ccccc1)c1ccccc1)NC[C@H]1CCCNC1

HCID11092454

未命名化合物

PRODUCTS

生成物

结构：CCC(C)CN1CCC[C@H](CNC(=O)CCCCCNC(=O)CC(c2ccccc2)(c2ccccc2)c2ccccc2)C1

HCID69100899

未命名化合物

PROCEDURE

实验过程

The title compound was prepared by a method similar to Step 3 of Example 17, using N-{6-{((3S)-3-piperidyl)methyl}amino-6-oxohexyl}-3,3,3-triphenylpropanamide and 2-methylbutanal. The compound was obtained as a white foamy substance.

WORKUP

后处理

customThe compound was obtained as a white foamy substance

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-f9e29ad3e87a4e738d4eb177a7019cde
来源数据集: uspto-grants-2008_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07452908B2
来源说明: uspto-grants-2008_11

反应 SMILES

[NH:1]1[CH2:6][CH2:5][CH2:4][C@H:3]([CH2:7][NH:8][C:9](=[O:38])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][C:16](=[O:37])[CH2:17][C:18]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:2]1.[CH3:39][CH:40]([CH2:43][CH3:44])[CH:41]=O>>[CH3:39][CH:40]([CH2:43][CH3:44])[CH2:41][N:1]1[CH2:6][CH2:5][CH2:4][C@H:3]([CH2:7][NH:8][C:9](=[O:38])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][C:16](=[O:37])[CH2:17][C:18]([C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=2)([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH2:2]1