Piconol → HCID 68702536, compound
Reaction equation
Cl[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9].[N:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[CH2:17][OH:18]>>[N:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[CH2:17][O:18][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9]Participants
3
Procedure
In accordance with the same procedures as in Preparation 2, except for using 4-chloro-3-nitropyridine prepared in Step 1 of Preparation 1 and 2-pyridyl carbinol, the titled compound was obtained as a yellow solid. (Yield: 68.3%)
Workup
- customIn accordance with the same procedures as in Preparation 2
Sources & evidence
- ORD record
- ord-ddb05b7ba499477a81ddc01253f5c64e
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07642269B2
Reaction notes
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