Benzyl Bromide → 4-Benzyl-2-chloro-pyrimidine
Reaction equation
[CH2:1](Br)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:9][C:10]1[N:15]=[C:14](Cl)[CH:13]=[CH:12][N:11]=1>>[Cl:9][C:10]1[N:15]=[C:14]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH:13]=[CH:12][N:11]=1Participants
3
Procedure
The title compound (quantitiative yield) was prepared from benzyl bromide (1.71 g, 1.19 ml, 10 mmol) and 2,4-dichloropyrimidine (1.49 g, 10 mmol) in a similar manner to Intermediate 2, and was used without purification.
Workup
- customwas used without purification
Sources & evidence
- ORD record
- ord-fbe8224fb98940a19e885c83a9c33465
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06319922B1
Reaction notes
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