HRID1243260

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：C=C(C)C(=O)OCCCCCCOc1ccc(C(=O)Oc2ccc3ccc(=O)oc3c2)cc1

HCID21251812

未命名化合物

结构：C=C(C)C(=O)OCCCCCCOc1c(OC)cc(-c2nc3ccccc3s2)cc1OC

HCID69584419

未命名化合物

PRODUCTS

生成物

结构：C=C(C)C(=O)OCCCCCCOc1c(OC)cc(-c2nc3ccccc3s2)cc1OC.C=C(C)C(=O)OCCCCCCOc1ccc(C(=O)Oc2ccc3ccc(=O)oc3c2)cc1

HCID87899487

未命名化合物

PROCEDURE

实验过程

Compound 26 was prepared by copolymerisation of 2-Methylacrylic acid 6-(4-benzothiazol-2-yl-2,6-dimethoxyphenoxy)hexyl ester with 4-[6-(methacryloyloxy)hexyloxy]benzoic acid 2-oxo-2H-chromen-7-yl ester in a method analogous to the copolymerisation step of Compound 25.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-bbcc5ba667164bb7aa430742b5f86860
来源数据集: uspto-grants-2006_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07118787B2
来源说明: uspto-grants-2006_10

反应 SMILES

[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:28]=[C:27]([O:29][CH3:30])[C:13]([O:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][O:21][C:22](=[O:26])[C:23]([CH3:25])=[CH2:24])=[C:12]([O:31][CH3:32])[CH:11]=1.[O:33]=[C:34]1[CH:43]=[CH:42][C:41]2[C:36](=[CH:37][C:38]([O:44][C:45](=[O:65])[C:46]3[CH:51]=[CH:50][C:49]([O:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][O:59][C:60](=[O:64])[C:61]([CH3:63])=[CH2:62])=[CH:48][CH:47]=3)=[CH:39][CH:40]=2)[O:35]1>>[O:33]=[C:34]1[CH:43]=[CH:42][C:41]2[C:36](=[CH:37][C:38]([O:44][C:45](=[O:65])[C:46]3[CH:51]=[CH:50][C:49]([O:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][O:59][C:60](=[O:64])[C:61]([CH3:63])=[CH2:62])=[CH:48][CH:47]=3)=[CH:39][CH:40]=2)[O:35]1.[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:11]=[C:12]([O:31][CH3:32])[C:13]([O:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][O:21][C:22](=[O:26])[C:23]([CH3:25])=[CH2:24])=[C:27]([O:29][CH3:30])[CH:28]=1