3-Hydroxy-4-nitrobenzaldehyde → HCID 9903062, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[N+:10]([O-:12])=[O:11])[CH:5]=O.[C:13]1([CH2:19][CH2:20][CH2:21][NH:22][C:23](=[O:27])[CH2:24][C:25]#[N:26])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[OH:1][C:2]1[CH:3]=[C:4](/[CH:5]=[C:24](/[C:23]([NH:22][CH2:21][CH2:20][CH2:19][C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)=[O:27])\[C:25]#[N:26])[CH:7]=[CH:8][C:9]=1[N+:10]([O-:12])=[O:11]Participants
3
Procedure
M-39 was prepared with 3-hydroxy-4-nitro benzaldehyde and N-3-phenyl-n-propyl cyanoacetamide under similar conditions as described for M28.
Sources & evidence
- ORD record
- ord-7a5ea4fdb276498b908ff0ccedf0668d
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06596878B2
Reaction notes
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