1,2-Dibromoethane → HCID 86696142, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][S:9]([CH3:12])(=[O:11])=[O:10])[N:3]=1.Br[CH2:14][CH2:15]Br>>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([C:8]2([S:9]([CH3:12])(=[O:11])=[O:10])[CH2:15][CH2:14]2)[N:3]=1Participants
3
Procedure
The title compound was prepared from 2-bromo-6-methanesulfonylmethyl-pyridine and 1,2-dibromoethane following a procedure analogous to that described in Step 3 for Intermediate 4. Yield: 53% of theory; LC (method 3): tR=2.56 min; Mass spectrum (ESI+): m/z=276/278 (Br) [M+H]+.
Sources & evidence
- ORD record
- ord-6103a4b32fdd4ac1b561931e582e43e0
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08933072B2
Reaction notes
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