HCID 10913758, compound → HCID 10134929, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:8]2=[CH:9][CH:10]=[C:11]3[C:20]([N:19]=[C:18]4[C:13]([CH:14]=[CH:15][CH:16]=[C:17]4[C:21](O)=[O:22])=[N:12]3)=[C:7]2[CH:6]=[CH:5][N:4]=1.[CH3:24][N:25]([CH3:30])[CH2:26][C@H:27]([NH2:29])[CH3:28]>>[CH3:24][N:25]([CH3:30])[CH2:26][C@H:27]([NH:29][C:21]([C:17]1[C:18]2[C:13](=[N:12][C:11]3[C:20]([N:19]=2)=[C:7]2[CH:6]=[CH:5][N:4]=[C:3]([O:2][CH3:1])[C:8]2=[CH:9][CH:10]=3)[CH:14]=[CH:15][CH:16]=1)=[O:22])[CH3:28]Participants
3
Procedure
4-Methoxypyrido[4,3-α]phenazine-11-carboxylic acid (2-dimethylamino-1(R)-methylethyl)-amide was prepared from 4-methoxypyrido[4,3-α]phenazine-11-carboxylic acid (II.4) and (R)-N1,N1-Dimethyl-propane-1,2-diamine
Sources & evidence
- ORD record
- ord-de2cfdf969fc4cefb93f3b0cd19c3b86
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06552021B2
Reaction notes
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