5-Amino-3-methyl-9H-pyrido[2,3-b]indole-7-carbonitrile → 5-Amino-3-methyl-9H-pyrido[2,3-b]indole-7-carboxylic acid methyl ester
Reaction equation
[CH3:1][O:2][C:3](=[O:24])[C:4]1[CH:9]=[C:8]([N+:10]([O-])=O)[C:7]([C:13]2[C:14](F)=[N:15][CH:16]=[C:17]([CH3:19])[CH:18]=2)=[C:6]([N+:21]([O-])=O)[CH:5]=1.NC1C=C(C#N)C=C2C=1C1C=C(C)C=NC=1N2>>[CH3:1][O:2][C:3]([C:4]1[CH:9]=[C:8]2[C:7]([C:13]3[CH:18]=[C:17]([CH3:19])[CH:16]=[N:15][C:14]=3[NH:10]2)=[C:6]([NH2:21])[CH:5]=1)=[O:24]Participants
3
Procedure
The title compound was prepared in 88% yield from example Compound 128 according to the procedure outlined for the preparation of Compound 124. MS (ES) [m+H] calc'd for C14H13N3O2, 256; found 256.
Sources & evidence
- ORD record
- ord-0ea0c055e4db4ca19e6bb37ea984ed96
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318939B2
Reaction notes
Loading…