4-Bromo-3-iodopyridine → HCID 117667632, compound
Reaction equation
Br[C:2]1[CH:3]=[C:4]([C:8]2[CH:9]=[C:10]3[C:15](=[N:16][CH:17]=2)[N:14]([C:18]([NH2:20])=[O:19])[CH2:13][CH2:12][CH2:11]3)[CH:5]=[N:6][CH:7]=1.[Br:21]C1C=CN=CC=1I>>[Br:21][C:3]1[CH:2]=[CH:7][N:6]=[CH:5][C:4]=1[C:8]1[CH:9]=[C:10]2[C:15](=[N:16][CH:17]=1)[N:14]([C:18]([NH2:20])=[O:19])[CH2:13][CH2:12][CH2:11]2Participants
3
Procedure
6-(4-Bromo-pyridin-3-yl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid amide is synthesized using the same procedures for preparing 6-(5-bromo-pyridin-3-yl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid amide in Example 15, replacing 3,5-dibromo-pyridine with 4-bromo-3-iodo-pyridine.
Sources & evidence
- ORD record
- ord-1abdbfd96980471cb02e7f367c5bf5f7
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09181272B2
Reaction notes
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