3-Iodopyridine → HCID 67445886, 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:17]=[N:18][CH:19]=[CH:20][CH:21]=1>>[N:18]1[CH:19]=[CH:20][CH:21]=[C:16]([N:1]2[C:5]3=[N:6][CH:7]=[CH:8][CH:9]=[C:4]3[CH:3]=[C:2]2[C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH:17]=1Participants
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 3-iodopyridine. A yellow solid is obtained.
Workup
- customThis compound was prepared
- customobtained
- customA yellow solid is obtained
Sources & evidence
- ORD record
- ord-0dbb8801aab94344ae6600cc5f30f4b1
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08044066B2
Reaction notes
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