2-Iodopyridine → HCID 67444397, compound
Reaction equation
[NH:1]1[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[C:2]1[C:10]([O:12][CH2:13][CH3:14])=[O:11].I[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=1>>[N:17]1[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=1[N:1]1[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[C:2]1[C:10]([O:12][CH2:13][CH3:14])=[O:11]Participants
3
Procedure
This compound was prepared according to the experimental protocol described in Example 6.1, starting with ethyl 1H-pyrrolo[2,3-b]pyridine-2-carboxylate obtained according to the protocol described in step 3.2 and 2-iodopyridine. A beige-colored solid is obtained.
Workup
- customThis compound was prepared
- customobtained
- customA beige-colored solid is obtained
Sources & evidence
- ORD record
- ord-5972979bfe0d46459c9c0c3fbf8cac73
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08044066B2
Reaction notes
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