HRID1027671

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID6140

L-Phenylalanine

C9H11NO2

$结构：CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)NC(CC(C)C)C(=O)Nc1ccc(O)c(C(=O)O)c1$

HCID44626054

未命名化合物

PRODUCTS

生成物

$结构：CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)NC(Cc1ccccc1)C(=O)Nc1ccc(O)c(C(=O)O)c1$

HCID59193234

未命名化合物

PROCEDURE

实验过程

5-(2-(4Z,7Z,10Z,13Z,16Z,19Z)-Docosa-4,7,10,13,16,19-hexaenamido-3-phenylpropanamido)-2-hydroxybenzoic acid was prepared in a similar fashion as 5-(2-(4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamido-4-methylpentanamido)-2-hydroxybenzoic acid, using the appropriate phenylalanine starting material. Mass calculated for C38H46N2O5=610.78. found: [M−H]+=609.3.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-dfbf5561a26441f99d0c7af355293152
来源数据集: uspto-grants-2014_05
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08735379B2
来源说明: uspto-grants-2014_05

反应 SMILES

[C:1]([NH:24][CH:25]([CH2:39][CH:40]([CH3:42])[CH3:41])[C:26]([NH:28][C:29]1[CH:30]=[CH:31][C:32]([OH:38])=[C:33]([CH:37]=1)[C:34]([OH:36])=[O:35])=[O:27])(=[O:23])[CH2:2][CH2:3]/[CH:4]=[CH:5]\[CH2:6]/[CH:7]=[CH:8]\[CH2:9]/[CH:10]=[CH:11]\[CH2:12]/[CH:13]=[CH:14]\[CH2:15]/[CH:16]=[CH:17]\[CH2:18]/[CH:19]=[CH:20]\[CH2:21][CH3:22].N[C@H:44]([C:52](O)=O)[CH2:45]C1C=CC=CC=1>>[C:1]([NH:24][CH:25]([CH2:39][C:40]1[CH:41]=[CH:52][CH:44]=[CH:45][CH:42]=1)[C:26]([NH:28][C:29]1[CH:30]=[CH:31][C:32]([OH:38])=[C:33]([CH:37]=1)[C:34]([OH:36])=[O:35])=[O:27])(=[O:23])[CH2:2][CH2:3]/[CH:4]=[CH:5]\[CH2:6]/[CH:7]=[CH:8]\[CH2:9]/[CH:10]=[CH:11]\[CH2:12]/[CH:13]=[CH:14]\[CH2:15]/[CH:16]=[CH:17]\[CH2:18]/[CH:19]=[CH:20]\[CH2:21][CH3:22]