HRID2194301

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID22344597

未命名化合物

PRODUCTS

生成物

结构：COc1cc(Cn2c3ccccc3c3c(OC(C(=O)O)c4ccccc4)cccc32)ccc1OCc1nc(-c2ccco2)oc1C

HCID11563484

未命名化合物

PROCEDURE

实验过程

The subject compound was prepared by performing the same operation as that of the example 3 by using 2-(9H-carbazole-4-yloxy)-2-phenylacetic acid prepared by the reference 21 instead of 2-(9H-carbazole-4-yloxy)-2-methylpropionic acid used in the example 3, and using 4-((4-(chloromethyl)-2-methoxyphenoxy)methyl)-2-(furan-2-yl)-5-methyloxazole prepared by the reference 2 instead of 4-((4-(chloromethyl)-2-methoxyphenoxy)methyl)-5-methyl-2-phenyloxazole.

WORKUP

后处理

customThe subject compound was prepared

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0716b7fdc6c34585bcce96f1bb025865
来源数据集: uspto-grants-2012_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08329913B2
来源说明: uspto-grants-2012_12

反应 SMILES

[CH:1]1[C:13]2[NH:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[C:4]([O:14][CH:15]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:16]([OH:18])=[O:17])=[CH:3][CH:2]=1.C1C2NC3C(=CC=CC=3)C=2C(OC(C)(C)C(O)=O)=CC=1.Cl[CH2:46][C:47]1[CH:65]=[CH:64][C:50]([O:51][CH2:52][C:53]2[N:54]=[C:55]([C:59]3[O:60][CH:61]=[CH:62][CH:63]=3)[O:56][C:57]=2[CH3:58])=[C:49]([O:66][CH3:67])[CH:48]=1.ClCC1C=CC(OCC2N=C(C3C=CC=CC=3)OC=2C)=C(OC)C=1>>[O:60]1[CH:61]=[CH:62][CH:63]=[C:59]1[C:55]1[O:56][C:57]([CH3:58])=[C:53]([CH2:52][O:51][C:50]2[CH:64]=[CH:65][C:47]([CH2:46][N:12]3[C:13]4[CH:1]=[CH:2][CH:3]=[C:4]([O:14][CH:15]([C:19]5[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=5)[C:16]([OH:18])=[O:17])[C:5]=4[C:6]4[C:11]3=[CH:10][CH:9]=[CH:8][CH:7]=4)=[CH:48][C:49]=2[O:66][CH3:67])[N:54]=1