Chlorosuccinimide → 2-Amino-4-(5-chloro-furan-2-yl)-6-(3,5-dimethyl-pyridin-2-ylmethoxy)-pyrimidine-5-carbonitrile
Reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([O:8][CH2:9][C:10]2[C:15]([CH3:16])=[CH:14][C:13]([CH3:17])=[CH:12][N:11]=2)[C:5]([C:18]#[N:19])=[C:4]([C:20]2[O:21][CH:22]=[CH:23][CH:24]=2)[N:3]=1.[Cl:25]N1C(=O)CCC1=O>CN(C=O)C>[NH2:1][C:2]1[N:3]=[C:4]([C:20]2[O:21][C:22]([Cl:25])=[CH:23][CH:24]=2)[C:5]([C:18]#[N:19])=[C:6]([O:8][CH2:9][C:10]2[C:15]([CH3:16])=[CH:14][C:13]([CH3:17])=[CH:12][N:11]=2)[N:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
From 2-amino-4-(3,5-dimethyl-pyridin-2-ylmethoxy)-6-furan-2-yl-pyrimidine-5-carbonitrile and N-chlorosuccinimide in DMF. ES-MS m/e (%): 358 (M{37Cl}+H+, 30), 356 (M{35Cl}+H+, 100).
Sources & evidence
- ORD record
- ord-3a40bda8dcbd440ebaaacfe50040d709
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06586441B2
Reaction notes
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