HRID735947

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID12370

1-Octyne

C8H14

结构：CCCCCCC#Cc1ccc(CN(Cc2ccc(Br)cc2)C(=O)C(=O)OCC)cc1

HCID67186239

未命名化合物

PRODUCTS

生成物

结构：CCCCCCC#Cc1ccc(CN(Cc2ccc(C#CCCCCCC)cc2)C(=O)C(=O)OCC)cc1

HCID67187698

未命名化合物

收率 32%

PROCEDURE

实验过程

The same procedure as employed in the preparation of Example 226 (step c) but using ethyl[(4-bromobenzyl)(4-oct-1-ynylbenzyl)amino](oxo)acetate and 1-octyne gave the title compound as a pale yellow oil (32%). 1H NMR (CDCl3, 300 MHz) δ 7.38 (m, 4H), 7.16 (d, 2H, J=8.3 Hz), 7.12 (d, 2H, J=7.9 Hz), 4.45 (s, 2H), 4.35 (q, 2H, J=7.2 Hz), 4.28 (s, 2H), 2.42 (t, 4H, J=7.1 Hz), 1.62 (m, 4H), 1.47 (m, 4H), 1.33 (m, 11H), 0.92 (t, 6H, J=6.8 Hz). M+(LC/MS(ESI)): 514.0. HPLC (Condition A), Rt: 6.54 min (HPLC purity: 99.3%).

WORKUP

后处理

customThe same procedure as employed in the preparation of Example 226 (step c)

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-dfd3d5eb7fc940a9ae273620975fe95f
来源数据集: uspto-grants-2009_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07592477B2
来源说明: uspto-grants-2009_09

反应 SMILES

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