N,N-Dimethylethylenediamine → HCID 178498218, compound
Reaction equation
[CH:1]([C:3]1[C:16]([OH:17])=[C:15]([CH3:18])[C:14]([OH:19])=[C:13]2[C:4]=1[N:5]=[C:6]1[C:11](=[N:12]2)[C:10]([C:20]([O:22][CH3:23])=[O:21])=[CH:9][CH:8]=[C:7]1[OH:24])=O.[CH3:25][N:26]([CH3:30])[CH2:27][CH2:28][NH2:29]>O1CCCC1>[CH3:25][N:26]([CH3:30])[CH2:27][CH2:28][N:29]=[CH:1][C:3]1[C:16]([OH:17])=[C:15]([CH3:18])[C:14]([OH:19])=[C:13]2[C:4]=1[N:5]=[C:6]1[C:11](=[N:12]2)[C:10]([C:20]([O:22][CH3:23])=[O:21])=[CH:9][CH:8]=[C:7]1[OH:24]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
6-Formyl-4,7,9-trihydroxy-8-methyl-1-phenazinecarboxylic acid, methyl ester (500 mg, 1.52 mmol) was suspended in 50 ml of tetrahydrofuran and 2-(dimethylamino)ethylamine (160 mg, 1.83 mmol) was added dropwise with stirring to produce a deep purple solution. After about 20 minutes at room temperature, an orange precipitate formed and the reaction mixture gradually developed an orange color.
Workup
- customto produce a deep purple solution
- customan orange precipitate formed
Sources & evidence
- ORD record
- ord-8a1d918d776f4fba82aa28bf0533b5cd
- Source dataset
- uspto-grants-1988_04
- Patent number
- US04738929
Reaction notes
Loading…