1H-1,2,4-Triazole → HCID 19067968, compound
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][N:5]1[C:14]2[C:9](=[C:10]([CH2:19][CH:20]=[CH2:21])[C:11]([OH:18])=[C:12]([CH2:15][CH:16]=[CH2:17])[CH:13]=2)[CH2:8][CH2:7][C:6]1=[O:22].[NH:23]1[CH:27]=[N:26][CH:25]=[N:24]1>>[CH2:19]([C:10]1[C:11]([OH:18])=[C:12]([CH2:15][CH:16]=[CH2:17])[CH:13]=[C:14]2[C:9]=1[CH2:8][CH2:7][C:6](=[O:22])[N:5]2[CH2:4][CH2:3][CH2:2][N:26]1[CH:25]=[N:24][N:23]=[CH:27]1)[CH:20]=[CH2:21]Participants
3
Procedure
1-(3-Chloropropyl)-5,7-diallyl-3,4-dihydro-6-hydroxy-2(1H)-quinolinone and 1H-1,2,4-triazole were reacted and treated similarly as in Example 71, there was obtained 5,7-diallyl-3,4-dihydro-6-hydroxy-1-[3-(1,2,4-triazol-4-yl)propyl]-2(1H)-quinolinone.
Workup
- additiontreated similarly as in Example 71
Sources & evidence
- ORD record
- ord-15335e55c4cd4a718195743c924419f0
- Source dataset
- uspto-grants-1998_07
- Patent number
- US05786367
Reaction notes
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