HRID61782

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID54578543

6-Bromo-7-methoxy-1,1-dimethyl-3,4-dihydronaphthalen-2(1H)-one

C13H15BrO2

结构：COc1ccc2c(c1)C(C)(C)c1[nH]c3cc(Br)ccc3c1C2=O

HCID66834292

未命名化合物

PRODUCTS

生成物

结构：COc1cc2c(cc1Br)Cc1c([nH]c3cc(Br)ccc13)C2(C)C.COc1cc2c(cc1Br)Cc1c([nH]c3cccc(Br)c13)C2(C)C

HCID67127783

未命名化合物

PROCEDURE

实验过程

Under the same conditions as the method for synthesizing Compound A4, the title compound was prepared (as a mixture) from Compound E1.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-4d4cd9bfe4fe432faf2e11f37194625c
来源数据集: uspto-grants-2016_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09440922B2
来源说明: uspto-grants-2016_09

反应 SMILES

[Br:1][C:2]1[CH:14]=[C:13]2[C:5]([C:6]3[C:7](=O)[C:8]4[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:9]=4[C:10]([CH3:16])([CH3:15])[C:11]=3[NH:12]2)=[CH:4][CH:3]=1.[Br:24][C:25]1[CH:26]=[C:27]2[C:32](=[CH:33][C:34]=1[O:35][CH3:36])[C:31]([CH3:38])([CH3:37])[C:30](=O)[CH2:29][CH2:28]2>>[Br:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:13]2[C:14]=1[C:6]1[CH2:7][C:8]3[CH:20]=[C:19]([Br:24])[C:18]([O:21][CH3:22])=[CH:17][C:9]=3[C:10]([CH3:15])([CH3:16])[C:11]=1[NH:12]2.[Br:1][C:2]1[CH:14]=[C:13]2[C:5]([C:29]3[CH2:28][C:27]4[CH:26]=[C:25]([Br:24])[C:34]([O:35][CH3:36])=[CH:33][C:32]=4[C:31]([CH3:38])([CH3:37])[C:30]=3[NH:12]2)=[CH:4][CH:3]=1