Triethanolamine → HCID 19915072, compound
Reaction equation
[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]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
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.
Sources & evidence
- ORD record
- ord-f84dc19713004c8ab05cc54d8310a3c9
- Source dataset
- uspto-grants-1990_03
- Patent number
- US04906285
Reaction notes
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