HRID264081

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID32484

2,6-Diisopropylaniline

C12H19N

HCID84271

2,4,6-Trimethoxyaniline

C9H13NO3

结构：CCCCCCCCCCCCc1nnn(C(C(=O)O)c2ccccc2)n1

HCID10523338

未命名化合物

HCID21469529

未命名化合物

PRODUCTS

生成物

结构：CCCCCCCCCCCCc1nnn(C(C(=O)Nc2c(OC)cc(OC)cc2OC)c2ccccc2)n1

HCID10324930

未命名化合物

PROCEDURE

实验过程

When in the general procedure of Example 88 an appropriate amount of (±)-5-dodecyl-α-phenyl-2H-tetrazole-2-acetic acid was substituted for 5-decyl-2H-tetrazole-2-acetic acid and 2,4,6-trimethoxyaniline was substituted for 2,6-diisopropylaniline, the title compound was obtained, mp 141°-145° C.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-3af9f5debf194fb7aeb00a6f22474de1
来源数据集: uspto-grants-1997_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05646170
来源说明: uspto-grants-1997_07

反应 SMILES

[CH2:1]([C:13]1[N:14]=[N:15][N:16]([CH:18]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:19]([OH:21])=O)[N:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].C(C1N=NN(CC(O)=O)N=1)CCCCCCCCC.[CH3:47][O:48][C:49]1[CH:55]=[C:54]([O:56][CH3:57])[CH:53]=[C:52]([O:58][CH3:59])[C:50]=1[NH2:51].C(C1C=CC=C(C(C)C)C=1N)(C)C>>[CH2:1]([C:13]1[N:14]=[N:15][N:16]([CH:18]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:19]([NH:51][C:50]2[C:52]([O:58][CH3:59])=[CH:53][C:54]([O:56][CH3:57])=[CH:55][C:49]=2[O:48][CH3:47])=[O:21])[N:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]