4,6-Dichloropyrimidine → HCID 66991795, compound
Reaction equation
Cl[C:2]1[CH:7]=[C:6](Cl)[N:5]=[CH:4][N:3]=1.[NH2:9][C:10]1[C:11]([CH3:17])=[C:12]([OH:16])[CH:13]=[CH:14][CH:15]=1>>[OH:16][C:12]1[C:11]([CH3:17])=[C:10]([NH:9][C:2]2[CH:7]=[C:6]([NH:9][C:10]3[CH:15]=[CH:14][CH:13]=[C:12]([OH:16])[C:11]=3[CH3:17])[N:5]=[CH:4][N:3]=2)[CH:15]=[CH:14][CH:13]=1Participants
3
Procedure
This compound was obtained (yield 40%) based on the method described in Production Example 2B using 4,6-dichloropyrimidine instead of the 4,6-dichloro-2-ethylpyrimidine, and using 3-amino-2-methylphenol instead of the 3-aminophenol.
Workup
- customThis compound was obtained (yield 40%)
Sources & evidence
- ORD record
- ord-cb517cf88bc54935ba4e25b3427af935
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08003645B2
Reaction notes
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