2,4-Dichloropyrimidine → 5-(2-Chloro-pyrimidin-4-yl)-2-methoxy-benzaldehyde
Reaction equation
[Cl:1][C:2]1[N:7]=[C:6](Cl)[CH:5]=[CH:4][N:3]=1.[CH:9]([C:11]1[CH:12]=[C:13](B(O)O)[CH:14]=[CH:15][C:16]=1[O:17][CH3:18])=[O:10]>>[Cl:1][C:2]1[N:7]=[C:6]([C:13]2[CH:14]=[CH:15][C:16]([O:17][CH3:18])=[C:11]([CH:12]=2)[CH:9]=[O:10])[CH:5]=[CH:4][N:3]=1Participants
3
Procedure
2,4 dichloropyrimidine and 3-formyl 4-methoxy phenyl boronic acid were coupled following procedure A. LC-MS showed the product was >95% pure and had the expected M+H+ of 249.
Sources & evidence
- ORD record
- ord-8ef3cb688d8745649ceef176d6aa4eec
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07732444B2
Reaction notes
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