2-Chloro-4,5,6-trimethylpyrimidine → 2-Chloro-5-ethyl-4,6-dimethylpyrimidine
Reaction equation
[Cl:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5]([CH3:9])=[C:4]([CH3:10])[N:3]=1.[CH3:11]C1C(C)=C(C)N=C(O)N=1>>[Cl:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5]([CH2:9][CH3:11])=[C:4]([CH3:10])[N:3]=1Participants
3
Procedure
The title compound was prepared in a manner analogous to Intermediate 17, substituting 5-ethyl-4,6-dimethylpyrimidin-2-ol for 4,5,6-trimethylpyrimidin-2-ol. MS (ESI): mass calculated for C8H11ClN2, 170.06, m/z found 171.1 [M+1]+. 1H NMR (500 MHz, CDCl3): 2.65 (q, J=7.6 Hz, 2H), 2.50 (s, 6H), 1.15 (t, J=7.6 Hz, 3H).
Sources & evidence
- ORD record
- ord-0a0ecd69b8db4e80abf9b58445d6ef10
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062044B2
Reaction notes
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