2,3-Diaminopyridine → HCID 13282064, compound
Reaction equation
[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[CH:4][N:3]=1.[CH3:9][O:10][C:11]1[CH:12]=[C:13]([CH:17]=[CH:18][C:19]=1[NH:20][S:21]([CH3:24])(=[O:23])=[O:22])[C:14](O)=O>>[CH3:9][O:10][C:11]1[CH:12]=[C:13]([C:14]2[NH:8][C:7]3[C:2]([N:1]=2)=[N:3][CH:4]=[CH:5][CH:6]=3)[CH:17]=[CH:18][C:19]=1[NH:20][S:21]([CH3:24])(=[O:23])=[O:22]Participants
3
Procedure
Prepared analogously to Example 14 from 2,3-diaminopyridine and 3-methoxy-4-methanesulfonylamino-benzoic acid.
Sources & evidence
- ORD record
- ord-ca76b9db7f7f4ba7ba8d2803f0b55770
- Source dataset
- uspto-grants-1987_09
- Patent number
- US04696931
Reaction notes
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