HRID2284206

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2764335

4-(1,4-Dioxa-8-azaspiro[4.5]decan-8-yl)benzaldehyde

C14H17NO3

结构：O=C(Nc1ccc([N+](=O)[O-])c([N+](=O)[O-])c1)c1ccc(N2CCOCC2)cc1

HCID86673955

未命名化合物

PRODUCTS

生成物

结构：O=C(Nc1ccc2[nH]c(-c3ccc(N4CCC5(CC4)OCCO5)cc3)nc2c1)c1ccc(N2CCOCC2)cc1

HCID178521802

未命名化合物

PROCEDURE

实验过程

Compound 413 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(4-morpholinobenzoyl)aniline and 4-(1,4-dioxa-8-azaspiro[4,5]decan-8-yl)benzaldehyde. [M+H]+ calcd for C31H33N5O4: 540.25; found: 540.05.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-cc03c1c8195844f5a39d03e104f440bb
来源数据集: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09144557B2
来源说明: uspto-grants-2015_09

反应 SMILES

[N+:1]([C:4]1[CH:5]=[C:6]([CH:22]=[CH:23][C:24]=1[N+:25]([O-])=O)[NH:7][C:8](=[O:21])[C:9]1[CH:14]=[CH:13][C:12]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)=[CH:11][CH:10]=1)([O-])=O.[O:28]1[C:32]2([CH2:37][CH2:36][N:35]([C:38]3[CH:45]=[CH:44][C:41]([CH:42]=O)=[CH:40][CH:39]=3)[CH2:34][CH2:33]2)[O:31][CH2:30][CH2:29]1>>[O:31]1[C:32]2([CH2:33][CH2:34][N:35]([C:38]3[CH:45]=[CH:44][C:41]([C:42]4[NH:25][C:24]5[CH:23]=[CH:22][C:6]([NH:7][C:8](=[O:21])[C:9]6[CH:14]=[CH:13][C:12]([N:15]7[CH2:20][CH2:19][O:18][CH2:17][CH2:16]7)=[CH:11][CH:10]=6)=[CH:5][C:4]=5[N:1]=4)=[CH:40][CH:39]=3)[CH2:36][CH2:37]2)[O:28][CH2:29][CH2:30]1