HRID1493391

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID13478

Triethyl 1,3,5-triazine-2,4,6-tricarboxylate

C12H15N3O6

结构：CON1C(C)(C)CC(NC2CC(C)(C)N(OC)C(C)(C)C2)CC1(C)C

HCID19831392

未命名化合物

PRODUCTS

生成物

结构：CON1C(C)(C)CC(N(C(=O)c2nc(C(=O)N(C3CC(C)(C)N(OC)C(C)(C)C3)C3CC(C)(C)N(OC)C(C)(C)C3)nc(C(=O)N(C3CC(C)(C)N(OC)C(C)(C)C3)C3CC(C)(C)N(OC)C(C)(C)C3)n2)C2CC(C)(C)N(OC)C(C)(C)C2)CC1(C)C

HCID19831388

未命名化合物

PROCEDURE

实验过程

The title compound is prepared by the reaction of triethyl 1,3,5-triazine-2,4,6-tricarboxylate and bis(1-methoxy-2,2,6,6-tetramethylpiperidin-4-yl)amine.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-c21249ad2cd64ccdbb6726c70e7cc8e7
来源数据集: uspto-grants-1991_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05021483
来源说明: uspto-grants-1991_06

反应 SMILES

[N:1]1[C:6]([C:7]([O:9]CC)=O)=[N:5][C:4]([C:12]([O:14]CC)=O)=[N:3][C:2]=1[C:17]([O:19]CC)=O.[CH3:22][O:23][N:24]1[C:29]([CH3:31])([CH3:30])[CH2:28][CH:27]([NH:32][CH:33]2[CH2:38][C:37]([CH3:40])([CH3:39])[N:36]([O:41][CH3:42])[C:35]([CH3:44])([CH3:43])[CH2:34]2)[CH2:26][C:25]1([CH3:46])[CH3:45]>>[CH3:42][O:41][N:36]1[C:37]([CH3:40])([CH3:39])[CH2:38][CH:33]([N:32]([CH:27]2[CH2:28][C:29]([CH3:31])([CH3:30])[N:24]([O:23][CH3:22])[C:25]([CH3:46])([CH3:45])[CH2:26]2)[C:17]([C:2]2[N:1]=[C:6]([C:7]([N:32]([CH:27]3[CH2:28][C:29]([CH3:31])([CH3:30])[N:24]([O:23][CH3:22])[C:25]([CH3:46])([CH3:45])[CH2:26]3)[CH:33]3[CH2:38][C:37]([CH3:40])([CH3:39])[N:36]([O:41][CH3:42])[C:35]([CH3:44])([CH3:43])[CH2:34]3)=[O:9])[N:5]=[C:4]([C:12]([N:32]([CH:33]3[CH2:34][C:35]([CH3:44])([CH3:43])[N:36]([O:41][CH3:42])[C:37]([CH3:40])([CH3:39])[CH2:38]3)[CH:27]3[CH2:26][C:25]([CH3:46])([CH3:45])[N:24]([O:23][CH3:22])[C:29]([CH3:30])([CH3:31])[CH2:28]3)=[O:14])[N:3]=2)=[O:19])[CH2:34][C:35]1([CH3:44])[CH3:43]