1-Bromo-2-Chloroethane → HCID 18936671, compound
Reaction equation
[SH:1][C:2]1[N:7]2[CH:8]=[CH:9][N:10]=[C:6]2[CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.Br[CH2:19][CH2:20][Cl:21]>>[Cl:21][CH2:20][CH2:19][S:1][C:2]1[N:7]2[CH:8]=[CH:9][N:10]=[C:6]2[CH:5]=[CH:4][CH:3]=1Participants
4
Procedure
Using 3.0 g (20 mmol) of 5-mercaptoimidazo[1,2-a]pyridine, 2.79 ml (20 mmol) of triethylamine and 1.66 ml (20 mmol) of 1-bromo-2-chloroethane, the same procedure as in Reference Example 1 was followed, to yield 2.29 g (54.0%, light brown oily substance) of the desired product.
Sources & evidence
- ORD record
- ord-8f8c17b413ef4e6f95a3c32c2659828e
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05840732
Reaction notes
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