HRID1164720

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7618

Triethanolamine

C6H15NO3

结构：COc1cc(OC)nc(Oc2cccc(Oc3nc(OC)cc(OC)n3)c2C(=O)O)n1

HCID443031

Bispyribac

C19H18N4O8

PRODUCTS

生成物

结构：COc1cc(OC)nc(Oc2cccc(Oc3nc(OC)cc(OC)n3)c2C(=O)[O-])n1.OCC[NH+](CCO)CCO

HCID19915072

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID8028

Tetrahydrofuran

C4H8O

PROCEDURE

实验过程

2,6-bis[(4,6-dimethoxypyrimidin-2-yl)oxy]benzoic acid (2.0 g) and triethanolamine (0.7 g) were dissolved in 30 ml of THF, and the solution was stirred at room temperature for 12 hours.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-f84dc19713004c8ab05cc54d8310a3c9
来源数据集: uspto-grants-1990_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04906285
来源说明: uspto-grants-1990_03

反应 SMILES

[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[N:6]=[C:5]([O:11][C:12]2[CH:20]=[CH:19][CH:18]=[C:17]([O:21][C:22]3[N:27]=[C:26]([O:28][CH3:29])[CH:25]=[C:24]([O:30][CH3:31])[N:23]=3)[C:13]=2[C:14]([OH:16])=[O:15])[N:4]=1.[N:32]([CH2:39][CH2:40][OH:41])([CH2:36][CH2:37][OH:38])[CH2:33][CH2:34][OH:35]>C1COCC1>[CH3:29][O:28][C:26]1[CH:25]=[C:24]([O:30][CH3:31])[N:23]=[C:22]([O:21][C:17]2[CH:18]=[CH:19][CH:20]=[C:12]([O:11][C:5]3[N:4]=[C:3]([O:2][CH3:1])[CH:8]=[C:7]([O:9][CH3:10])[N:6]=3)[C:13]=2[C:14]([O-:16])=[O:15])[N:27]=1.[OH:35][CH2:34][CH2:33][NH+:32]([CH2:39][CH2:40][OH:41])[CH2:36][CH2:37][OH:38]