HRID832878

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID313

Hydrochloric Acid

ClH

HCID887

Methanol

CH4O

HCID8857

Ethyl acetate

C4H8O2

2 次

结构：CNC(=O)c1ccc2c(C)cc(=O)n(CCN3CCC(N(Cc4ccc5c(c4)OCCO5)C(=O)OC(C)(C)C)CC3)c2c1

HCID59398071

tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(4-methyl-7-((methylamino) carbonyl)-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate

C33H42N4O6

PRODUCTS

生成物

HCID313

Hydrochloric Acid

ClH

结构：CNC(=O)c1ccc2c(C)cc(=O)n(CCN3CCC(NCc4ccc5c(c4)OCCO5)CC3)c2c1

HCID59397868

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-cc6222011a3b4487a842bbee749442ef
来源数据集: Test data from https://doi.org/10.1039/C8SC04228D
DOI: 10.1039/C8SC04228D
来源说明: Test data from https://doi.org/10.1039/C8SC04228D

反应 SMILES

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