3-Bromo-1,1,1-Trifluoro-2-Propanol → 6-[N-(5-Bromo-2-(3,3,3-trifluoro-2-hydroxypropoxy)benzyl)-N-ethylamino]-3-cyanopyridazine
Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([OH:20])=[C:6]([CH:19]=1)[CH2:7][N:8]([C:11]1[N:16]=[N:15][C:14]([C:17]#[N:18])=[CH:13][CH:12]=1)[CH2:9][CH3:10].[F:21][C:22]([F:28])([F:27])[CH:23]([OH:26])[CH2:24]Br>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:20][CH2:24][CH:23]([OH:26])[C:22]([F:28])([F:27])[F:21])=[C:6]([CH:19]=1)[CH2:7][N:8]([C:11]1[N:16]=[N:15][C:14]([C:17]#[N:18])=[CH:13][CH:12]=1)[CH2:9][CH3:10]Participants
3
Procedure
The title compound was prepared by reacting 6-[N-(5-bromo-2-hydroxybenzyl)-N-ethylamino]-3-cyanopyridazine with 1,1,1-trifluoro-3-bromo-propan-2-ol using a method similar to that of reference example 4.
Sources & evidence
- ORD record
- ord-8cd8a96c9745433e9e303df85bca95c8
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05994353
Reaction notes
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