6-Methoxy-2,3-pyridinediamine HCl → HCID 70419800, compound
Reaction equation
[ClH:1].Cl.[NH2:3][C:4]1[C:9]([NH2:10])=[CH:8][CH:7]=[C:6]([O:11][CH3:12])[N:5]=1.[CH2:13]([O:16][C:17]1[CH:25]=[C:24]([S:26][CH3:27])[CH:23]=[CH:22][C:18]=1[C:19](O)=O)[CH2:14][CH3:15]>>[ClH:1].[CH2:13]([O:16][C:17]1[CH:25]=[C:24]([S:26][CH3:27])[CH:23]=[CH:22][C:18]=1[C:19]1[NH:10][C:9]2[C:4]([N:3]=1)=[N:5][C:6]([O:11][CH3:12])=[CH:7][CH:8]=2)[CH2:14][CH3:15]Participants
3
Procedure
Prepared analogously to Example 5 from 2,3-diamino-6-methoxypyridine dihydrochloride and 2-propoxy-4-methylmercapto-benzoic acid.
Sources & evidence
- ORD record
- ord-42289bdb3bd249a6a417937c8b9e169e
- Source dataset
- uspto-grants-1988_02
- Patent number
- US04722929
Reaction notes
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