HRID1217729

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

HCID57930076

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

C11H19N3O2

HCID66673002

5-Pyrimidinol, 2-[4-(methylsulfonyl)phenyl]-

C11H10N2O3S

PRODUCTS

生成物

结构：CC(C)c1noc(N2CCC(COc3cnc(-c4ccc(S(C)(=O)=O)cc4)nc3)CC2)n1

HCID24993407

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-65107229ebc6492994574c7760e91215
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (5/10)

反应 SMILES

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