5-Diethylamino-2-nitrosophenol hydrochloride → HCID 22116511, compound
Reaction equation
Cl.[CH2:2]([N:4]([CH2:14][CH3:15])[C:5]1[CH:6]=[CH:7][C:8]([N:12]=O)=[C:9]([OH:11])[CH:10]=1)[CH3:3].[OH:16][C:17]1[C:26]2[C:21](=[CH:22][C:23]([C:27]([OH:29])=[O:28])=[CH:24][CH:25]=2)[CH:20]=[CH:19][CH:18]=1>>[CH2:2]([N:4]([CH2:14][CH3:15])[C:5]1[CH:10]=[C:9]2[C:8](=[CH:7][CH:6]=1)[N:12]=[C:20]1[C:19](=[CH:18][C:17](=[O:16])[C:26]3[CH:25]=[CH:24][C:23]([C:27]([OH:29])=[O:28])=[CH:22][C:21]=31)[O:11]2)[CH3:3]Participants
3
Procedure
This was made similarly to the hydroxy derivative above except that the starting materials were 5-diethylamino-2-nitrosophenol hydrochloride and 1-hydroxynaphthalene-6-carboxylic acid.
Sources & evidence
- ORD record
- ord-8efb153fb83b4355b87824c9a52576ac
- Source dataset
- uspto-grants-2000_12
- Patent number
- US06166202
Reaction notes
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