2-Fluoropyridine → HCID 11624921, compound
Reaction equation
F[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[N:8]1[C:16]2[C:11](=[N:12][CH:13]=[CH:14][CH:15]=2)[S:10][C:9]=1[NH2:17].Cl[C:19]1[C:28]2[C:23](=[CH:24][CH:25]=[C:26]([OH:29])[CH:27]=2)[N:22]=[CH:21][N:20]=1>>[N:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[O:29][C:26]1[CH:27]=[C:28]2[C:23](=[CH:24][CH:25]=1)[N:22]=[CH:21][N:20]=[C:19]2[NH:17][C:9]1[S:10][C:11]2[C:16]([N:8]=1)=[CH:15][CH:14]=[CH:13][N:12]=2Participants
4
Procedure
The compound of Example 82 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-fluoropyridine, thiazolo[5,4-b]pyridin-2-yl-amine and 4-chloro-6-hydroxy-quinazoline.
Sources & evidence
- ORD record
- ord-1adc0d726b0d4bcaa243688b4c863185
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07687502B2
Reaction notes
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