HRID569678

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11067566

1,3-Benzenediamine, N,N,N',N'-tetrabutyl-

C22H40N2

结构：CCn1c2ccccc2c2cc(C3OC(=O)c4cc(N(C)C)ccc43)ccc21

HCID13651732

未命名化合物

PRODUCTS

生成物

结构：CCN(CC)c1ccc(C(c2ccc(N(C)C)cc2C(=O)O)c2ccc(N(C)C)cc2N(C)C)cc1

HCID20147814

未命名化合物

PROCEDURE

实验过程

Employing a procedure similar to that described in Example 1, part B above, 3-(9-ethyl-3-carbazolyl)-6-dimethylaminophthalide from A is interacted with N,N,N',N'-tetrabutyl-m-phenylenediamine to obtain 2-[α-(9-ethyl-3-carbazolyl)]-α-[2,4-bis(dibutylamino)phenyl]methyl-5-dimethylaminobenzoic acid (Formula III: R=CH3 ; X=H; Y=9-C2H5 -3-carbazolyl; Z=2,4-[(C4H9)2N]2C6H3).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-599f1830b9044aceab86db523bb79ced
来源数据集: uspto-grants-1988_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04732991
来源说明: uspto-grants-1988_03

反应 SMILES

[CH2:1]([N:3]1[C:15]2[CH:14]=[CH:13][C:12]([CH:16]3[C:25]4[C:20](=[CH:21][C:22]([N:26]([CH3:28])[CH3:27])=[CH:23][CH:24]=4)[C:18](=[O:19])[O:17]3)=[CH:11][C:10]=2C2[C:4]1=[CH:5]C=CC=2)[CH3:2].[CH2:29]([N:33]([CH2:49]CCC)[C:34]1[CH:39]=[CH:38][CH:37]=[C:36]([N:40]([CH2:45]CCC)[CH2:41]CCC)[CH:35]=1)CCC>>[CH3:49][N:33]([CH3:29])[C:34]1[CH:35]=[C:36]([N:40]([CH3:41])[CH3:45])[CH:37]=[CH:38][C:39]=1[CH:16]([C:25]1[CH:24]=[CH:23][C:22]([N:26]([CH3:28])[CH3:27])=[CH:21][C:20]=1[C:18]([OH:19])=[O:17])[C:12]1[CH:13]=[CH:14][C:15]([N:3]([CH2:4][CH3:5])[CH2:1][CH3:2])=[CH:10][CH:11]=1