HRID2136437

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

结构：Fc1ccc(-c2noc(-c3cc(F)cc(Br)c3)n2)nc1

HCID10290901

3-(5-Fluoro-2-pyridyl)-5-(3-bromo-5-fluorophenyl)-1,2,4-oxadiazole

C13H6BrF2N3O

结构：CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1

HCID11828117

4-(Tributylstannyl)-1-tritylimidazole

C34H44N2Sn

PRODUCTS

生成物

结构：Fc1ccc(-c2noc(-c3cc(F)cc(-c4cn(C(c5ccccc5)(c5ccccc5)c5ccccc5)cn4)c3)n2)nc1

HCID21942689

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-91710c83be6b4ca692e68917a804d919
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (4/10)

反应 SMILES

[CH2:1]([Sn:2]([CH2:3][CH2:4][CH2:5][CH3:30])([c:6]1[n:7][cH:8][n:9]([C:11]([c:12]2[cH:13][cH:14][cH:15][cH:16][cH:17]2)([c:18]2[cH:19][cH:20][cH:21][cH:22][cH:23]2)[c:24]2[cH:25][cH:26][cH:27][cH:28][cH:29]2)[cH:10]1)[CH2:31][CH2:32][CH2:33][CH3:34])[CH2:35][CH2:36][CH3:37].[F:38][c:39]1[cH:40][cH:41][c:42](-[c:45]2[n:46][o:47][c:48](-[c:50]3[cH:51][c:52]([Br:57])[cH:53][c:54]([F:56])[cH:55]3)[n:49]2)[n:43][cH:44]1.[O:58]1[CH2:59][CH2:60][CH2:61][CH2:62]1>>[c:6]1(-[c:52]2[cH:51][c:50](-[c:48]3[o:47][n:46][c:45](-[c:42]4[cH:41][cH:40][c:39]([F:38])[cH:44][n:43]4)[n:49]3)[cH:55][c:54]([F:56])[cH:53]2)[n:7][cH:8][n:9]([C:11]([c:12]2[cH:13][cH:14][cH:15][cH:16][cH:17]2)([c:18]2[cH:19][cH:20][cH:21][cH:22][cH:23]2)[c:24]2[cH:25][cH:26][cH:27][cH:28][cH:29]2)[cH:10]1