1,2-Dibromoethane → 1-(6-Chloropyridin-3-yl)cyclopropane-1-carbonitrile
Reaction equation
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][C:9]#[N:10])=[CH:4][CH:3]=1.Br[CH2:12][CH2:13]Br>>[Cl:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2([C:9]#[N:10])[CH2:13][CH2:12]2)=[CH:4][CH:3]=1Participants
3
Procedure
The title compound was prepared from (6-chloro-pyridin-3-yl)-acetonitrile and 1,2-dibromoethane following a procedure analogous to that described in Step 3 for Intermediate 4. Yield: 43% of theory; LC (method 3): tR=2.71 min; Mass spectrum (ESI+): m/z=179/181 (Cl) [M+H]+.
Sources & evidence
- ORD record
- ord-2dd4e1d4b9554990b7891a54ed1d5baa
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09090605B2
Reaction notes
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