HRID1480521

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC1=[N+](CCC(C)S(=O)(=O)[O-])c2ccc(S(=O)(=O)[O-])cc2C1(C)C.[Na+]

HCID87428036

未命名化合物

结构：CC1=Nc2c(cc(Cl)c[n+]2CCCCS(=O)(=O)[O-])C1(C)C

HCID89846329

未命名化合物

$结构：CC1(C)C2=CC=CN(CCCS(=O)(=O)[O-])C2=N/C1=C/C=C1\CCCC(/C=C/C2=[N+](CCCS(=O)(=O)[O-])c3ccc(S(=O)(=O)[O-])cc3C2(C)C)=C1Cl.[Na+].[Na+]$

HCID178422058

未命名化合物

PRODUCTS

生成物

$结构：CC1(C)C2=CC(Cl)=CN(CCCCS(=O)(=O)[O-])C2=N/C1=C/C=C1\CCC(/C=C/C2=[N+](CCCCS(=O)(=O)[O-])c3ccc(S(=O)(=O)[O-])cc3C2(C)C)=C1Cl.[Na+].[Na+]$

HCID178422044

未命名化合物

PROCEDURE

实验过程

Compound 39 is prepared analogously to compound 16, except with compound 38, compound 26, and the cyclopentyl chloro dye precursor as starting materials.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-801cc655270d4d68a96dde10579d2f13
来源数据集: uspto-grants-2016_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09408924B2
来源说明: uspto-grants-2016_08

反应 SMILES

[Cl:1][C:2]1=[C:3]([CH:28]=[CH:29][C:30]2[C:38]([CH3:40])([CH3:39])[C:37]3[C:32](=[CH:33][CH:34]=[C:35]([S:41]([O-:44])(=[O:43])=[O:42])[CH:36]=3)[N+:31]=2CCCS([O-])(=O)=O)[CH2:4][CH2:5][CH2:6]/[C:7]/1=C\C=C1/C(C)(C)C2C(=N/1)N(CCCS([O-])(=O)=O)C=CC=2.[Na+:52].[Na+].CC1C(C)(C)C2[C:57](=[CH:58][CH:59]=[C:60]([S:66]([O-:69])(=[O:68])=[O:67])C=2)[N+]=1CCC(S([O-])(=O)=O)C.[Na+].[Cl:79][C:80]1[CH:81]=[C:82]2[C:96]([CH3:98])([CH3:97])[C:95]([CH3:99])=[N:94][C:83]2=[N+:84]([CH2:86][CH2:87][CH2:88][CH2:89][S:90]([O-:93])(=[O:92])=[O:91])[CH:85]=1>>[Cl:1][C:2]1=[C:3]([CH:28]=[CH:29][C:30]2[C:38]([CH3:39])([CH3:40])[C:37]3[C:32](=[CH:33][CH:34]=[C:35]([S:41]([O-:44])(=[O:42])=[O:43])[CH:36]=3)[N+:31]=2[CH2:57][CH2:58][CH2:59][CH2:60][S:66]([O-:69])(=[O:68])=[O:67])[CH2:4][CH2:5]/[C:6]/1=[CH:7]\[CH:99]=[C:95]1/[C:96]([CH3:98])([CH3:97])[C:82]2[C:83](=[N:94]/1)[N:84]([CH2:86][CH2:87][CH2:88][CH2:89][S:90]([O-:93])(=[O:92])=[O:91])[CH:85]=[C:80]([Cl:79])[CH:81]=2.[Na+:52].[Na+:52]