Allyl iodide → HCID 11680159, compound
Reaction equation
[Cl:1][C:2]1[N:3]=[CH:4][CH:5]=[C:6]2[C:10]([CH3:11])=[C:9]([CH3:12])[NH:8][C:7]=12.[CH2:13](I)[CH:14]=[CH2:15]>>[CH2:15]([N:8]1[C:7]2=[C:2]([Cl:1])[N:3]=[CH:4][CH:5]=[C:6]2[C:10]([CH3:11])=[C:9]1[CH3:12])[CH:14]=[CH2:13]Participants
3
Procedure
In accordance with the same procedures as in Step 2 of Example 198, except for using 7-chloro-2,3-dimethyl-1H-pyrrolo[2,3-c]pyridine prepared in Step 1 of Example 198 and allyl iodide, the titled compound was obtained as a white solid. (Yield: 75%)
Sources & evidence
- ORD record
- ord-ba5368c122024ec4bbc7af6102552067
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188114B2
Reaction notes
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