2,3-Dichloropyridine → HCID 178478201, compound
Reaction equation
Cl[C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][N:3]=1.[NH2:9][C:10]1[NH:14][CH:13]=[N:12][N:11]=1.Cl[C:16]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([OH:26])[CH:24]=2)[N:19]=[CH:18][N:17]=1>>[Cl:8][C:7]1[C:2]([O:26][C:23]2[CH:24]=[C:25]3[C:20](=[CH:21][CH:22]=2)[N:19]=[CH:18][N:17]=[C:16]3[NH:9][C:10]2[NH:14][CH:13]=[N:12][N:11]=2)=[N:3][CH:4]=[CH:5][CH:6]=1Participants
4
Procedure
The compound of Example 118 was manufactured by the same method as in Example 95, by a similar method thereto or by a combination of such a method with a conventional method using 2,3-dichloropyridine, 3-amino-4H-[1,2,4]triazole and 4-chloro-6-hydroxy-quinazoline.
Sources & evidence
- ORD record
- ord-992feba3db3a4db2b39441986a0e5e3c
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07687502B2
Reaction notes
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