HRID2149538

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

HCID11357533

2-methylsulfonyl-4-benzyloxy-pyrimidine

C12H12N2O3S

结构：CC(C)(C)c1nc(C2CCC2)cc(N2CCN(CCCO)CC2)n1

HCID69026233

未命名化合物

HCID178418339

未命名化合物

PRODUCTS

生成物

结构：CC(C)(C)c1nc(C2CCC2)cc(N2CCN(CCCOc3nccc(OCc4ccccc4)n3)CC2)n1

HCID69027600

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-006743039a30453198737a7d8237ba1d
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

[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[n:6][c:7]([CH:21]2[CH2:22][CH2:23][CH2:24]2)[cH:8][c:9]([N:11]2[CH2:12][CH2:13][N:14]([CH2:17][CH2:18][CH2:19][OH:20])[CH2:15][CH2:16]2)[n:10]1.[CH2:25]([Li:26])[CH2:27][CH2:28][CH3:29].[CH2:30]([c:31]1[cH:32][cH:33][cH:34][cH:35][cH:36]1)[O:37][c:38]1[n:39][c:40]([S:44]([CH3:45])(=[O:46])=[O:47])[n:41][cH:42][cH:43]1.[O:48]1[CH2:49][CH2:50][CH2:51][CH2:52]1>>[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[n:6][c:7]([CH:21]2[CH2:22][CH2:23][CH2:24]2)[cH:8][c:9]([N:11]2[CH2:12][CH2:13][N:14]([CH2:17][CH2:18][CH2:19][O:20][c:40]3[n:39][c:38]([O:37][CH2:30][c:31]4[cH:32][cH:33][cH:34][cH:35][cH:36]4)[cH:43][cH:42][n:41]3)[CH2:15][CH2:16]2)[n:10]1