HRID2265373

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID17854458

未命名化合物

HCID21957887

N,N-Dimethyl-4-{[4-(propan-2-yl)anilino]methyl}aniline

C18H24N2

PRODUCTS

生成物

结构：CC(C)c1ccc(N(Cc2ccc(N(C)C)cc2)C(=O)C2CCc3c(OCc4ccccc4)cccc32)cc1

HCID59597231

未命名化合物

收率 110.9%

PROCEDURE

实验过程

By the reaction and treatment in the same manner as in Example 12 using 4-benzyloxyindan-1-carboxylic acid (0.7 g) and [(4-dimethylaminophenyl)methyl](4-isopropylphenyl)amine (0.7 g) as starting materials, 4-benzyloxy-N-[(4-dimethylaminophenyl)methyl]-N-(4-isopropylphenyl)indan-1-carboxamide (1.5 g) was obtained.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-7a412c7bcf0141a3950b2821eb72761c
来源数据集: uspto-grants-2010_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07855297B2
来源说明: uspto-grants-2010_12

反应 SMILES

[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][CH:15]=[C:14]2[C:10]=1[CH2:11][CH2:12][CH:13]2[C:18]([OH:20])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:21][N:22]([CH3:40])[C:23]1[CH:28]=[CH:27][C:26]([CH2:29][NH:30][C:31]2[CH:36]=[CH:35][C:34]([CH:37]([CH3:39])[CH3:38])=[CH:33][CH:32]=2)=[CH:25][CH:24]=1>>[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][CH:15]=[C:14]2[C:10]=1[CH2:11][CH2:12][CH:13]2[C:18]([N:30]([CH2:29][C:26]1[CH:25]=[CH:24][C:23]([N:22]([CH3:40])[CH3:21])=[CH:28][CH:27]=1)[C:31]1[CH:32]=[CH:33][C:34]([CH:37]([CH3:39])[CH3:38])=[CH:35][CH:36]=1)=[O:20])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1