HRID139842

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

HCID11776

Triphenylphosphine

C18H15P

HCID90295

6-Aminonaphthol

C10H9NO

HCID97268

Di-tert-butyl azodicarboxylate

C10H18N2O4

结构：CCOC(=O)c1[nH]c2c(Br)cccc2c1CCCOc1cccc2ccccc12

HCID68938945

Ethyl 7-bromo-3-[3-(1-naphthalenyloxy)propyl]-1H-indole-2-carboxylate

C24H22BrNO3

PRODUCTS

生成物

结构：CCOC(=O)c1[nH]c2c(Br)cccc2c1CCCOc1cccc2cc(N)ccc12

HCID68938609

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-12144f67f15846ec87ef4cb67e6d5133
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (9/10)

反应 SMILES

[Br:1][c:2]1[cH:3][cH:4][cH:5][c:6]2[c:7]([CH2:16][CH2:17][CH2:18][O:19][c:20]3[cH:21][cH:22][cH:23][c:24]4[cH:25][cH:26][cH:27][cH:28][c:29]34)[c:8]([C:11](=[O:12])[O:13][CH2:14][CH3:15])[nH:9][c:10]12.[N:61]([C:62]([O:63][C:64]([CH3:65])([CH3:66])[CH3:67])=[O:68])=[N:69][C:70]([O:71][C:72]([CH3:73])([CH3:74])[CH3:75])=[O:76].[NH2:30][c:31]1[cH:32][c:33]2[c:34]([cH:35][cH:36]1)[c:37]([OH:38])[cH:39][cH:40][cH:41]2.[O:77]1[CH2:78][CH2:79][CH2:80][CH2:81]1.[c:42]1([P:43]([c:44]2[cH:45][cH:46][cH:47][cH:48][cH:49]2)[c:50]2[cH:51][cH:52][cH:53][cH:54][cH:55]2)[cH:56][cH:57][cH:58][cH:59][cH:60]1>>[Br:1][c:2]1[cH:3][cH:4][cH:5][c:6]2[c:7]([CH2:16][CH2:17][CH2:18][O:19][c:20]3[cH:21][cH:22][cH:23][c:24]4[cH:25][c:26]([NH2:30])[cH:27][cH:28][c:29]34)[c:8]([C:11](=[O:12])[O:13][CH2:14][CH3:15])[nH:9][c:10]12