3-Hydroxypyridine → HCID 22759234, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.[C:8]([CH:11]([CH2:23][CH2:24][CH2:25][CH:26]([OH:36])[CH2:27]OC1C=CC(F)=CC=1)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])(=[O:10])[CH3:9]>>[C:8]([CH:11]([CH2:23][CH2:24][CH2:25][CH:26]([OH:36])[CH2:27][O:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])(=[O:10])[CH3:9]Participants
3
Procedure
The synthesis of this compound is carried out by the procedure of Example 1, Step E, except that an equivalent quantity of 3-hydroxypyridine is substituted for the 4-fluorophenol of Example 1, Step E.
Workup
- customThe synthesis of this compound
Sources & evidence
- ORD record
- ord-c18d174ed4f047479bf5cd8b1edcc599
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04020177
Reaction notes
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