HRID2127252

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

HCID11776

Triphenylphosphine

C18H15P

HCID643502

n-boc-4-hydroxypiperidine

C10H19NO3

结构：Oc1cc2nc(Nc3ccc(N4CCOCC4)cc3)ncc2cc1Br

HCID136029923

6-Bromo-2-[[4-(4-morpholinyl)phenyl]amino]-7-quinazolinol

C18H17BrN4O2

PRODUCTS

生成物

结构：CC(C)(C)OC(=O)N1CCC(Oc2cc3nc(Nc4ccc(N5CCOCC5)cc4)ncc3cc2Br)CC1

HCID67102395

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d57e38e5ba3e455dbf038c6c4705d879
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

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