HRID144731

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

HCID11776

Triphenylphosphine

C18H15P

HCID75555

未命名化合物

HCID2762865

6-Bromopyridin-3-ol

C5H4BrNO

HCID57930076

1-[3-(1-Methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinemethanol

C11H19N3O2

PRODUCTS

生成物

结构：CC(C)c1noc(N2CCC(COc3ccc(Br)nc3)CC2)n1

HCID86638738

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-a60b2be2409a418bb4edf9a75e705c1a
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:17][c:18]1[cH:19][cH:20][c:21]([OH:24])[cH:22][n:23]1.[CH2:58]1[O:59][CH2:60][CH2:61][CH2:62]1.[CH3:1][CH:2]([CH3:3])[c:4]1[n:5][o:6][c:7]([N:9]2[CH2:10][CH2:11][CH:12]([CH2:15][OH:16])[CH2:13][CH2:14]2)[n:8]1.[O:44]=[C:45]([O:46][CH:47]([CH3:48])[CH3:49])[N:50]=[N:51][C:52]([O:53][CH:54]([CH3:55])[CH3:56])=[O:57].[c:25]1([P:26]([c:27]2[cH:28][cH:29][cH:30][cH:31][cH:32]2)[c:33]2[cH:34][cH:35][cH:36][cH:37][cH:38]2)[cH:39][cH:40][cH:41][cH:42][cH:43]1>>[CH3:1][CH:2]([CH3:3])[c:4]1[n:5][o:6][c:7]([N:9]2[CH2:10][CH2:11][CH:12]([CH2:15][O:16][c:21]3[cH:20][cH:19][c:18]([Br:17])[n:23][cH:22]3)[CH2:13][CH2:14]2)[n:8]1