6-Chloro-3-[chloro(difluoro)methyl][1,2,4]triazolo[4,3-b]pyridazine → 6-(5-benzylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-3-[chloro(difluoro)methyl][1,2,4]triazolo[4,3-b]pyridazine
Reaction equation
Cl.[CH2:2]([N:9]1[CH2:16][CH:15]2[CH:11]([CH2:12][NH:13][CH2:14]2)[CH2:10]1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Cl[C:18]1[CH:19]=[CH:20][C:21]2[N:22]([C:24]([C:27]([Cl:30])([F:29])[F:28])=[N:25][N:26]=2)[N:23]=1>>[CH2:2]([N:9]1[CH2:10][CH:11]2[CH2:12][N:13]([C:18]3[CH:19]=[CH:20][C:21]4[N:22]([C:24]([C:27]([Cl:30])([F:29])[F:28])=[N:25][N:26]=4)[N:23]=3)[CH2:14][CH:15]2[CH2:16]1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1Participants
3
Procedure
A mixture of 2-benzylhexahydropyrrolo[3,4-c]pyrrole hydrochloride and 6-chloro-3-[chloro(difluoro)methyl]-[1,2,4]triazolo[4,3-b]pyridazine was allowed to react by an analogous method to Example 331 to give 6-(5-benzylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-3-[chloro(difluoro)methyl][1,2,4]triazolo[4,3-b]pyridazine in 66% yield.
Workup
- customto react by an analogous method to Example 331
Sources & evidence
- ORD record
- ord-e37d126d07a242088de91eb5ff5c34fd
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08003649B2
Reaction notes
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