HRID1370899

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID545831

3-Hydroxyoxolan-2-one

C4H6O3

结构：Cc1c(N(Cc2ccccc2)Cc2ccc(Oc3cccc(O)c3)cc2)cccc1[N+](=O)[O-]

HCID18512260

未命名化合物

PRODUCTS

生成物

结构：Cc1c(N(Cc2ccccc2)Cc2ccc(Oc3cccc(OC4CCOC4=O)c3)cc2)cccc1[N+](=O)[O-]

HCID18512398

未命名化合物

PROCEDURE

实验过程

The product from Example 61F and α-hydroxy-γ-butyrolactone were processed as described in Example 62A to provide the title compound.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-71a7b26be495419ab1841edcb86ea935
来源数据集: uspto-grants-2003_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06583180B2
来源说明: uspto-grants-2003_06

反应 SMILES

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