HRID1463692

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8113

Diethanolamine

C4H11NO2

结构：CC1(C)CC(CCCCNc2nc(Cl)nc(NCCCCC3CC(C)(C)N(OC4CCCCC4)C(C)(C)C3)n2)CC(C)(C)N1OC1CCCCC1

HCID22507638

未命名化合物

PRODUCTS

生成物

结构：CC1(C)CC(CCCCNc2nc(NCCCCC3CC(C)(C)N(OC4CCCCC4)C(C)(C)C3)nc(N(CCO)CCO)n2)CC(C)(C)N1OC1CCCCC1

HCID23372142

未命名化合物

PROCEDURE

实验过程

The title compound is prepared from the reaction of 2-chloro-4,6-bis[N-(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-1,3,5-triazine and diethanolamine according to the procedure of Example 1.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-7657634896d3452cb6cba8ff21c925cd
来源数据集: uspto-grants-1994_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05300544
来源说明: uspto-grants-1994_04

反应 SMILES

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