5-Hydrazinylquinoline → 1-[3-(Pyrrolidine-1-sulfonyl)-phenyl]-3-(2-quinolin-5-yl-2H-pyrazol-3-yl)-1H-pyridazin-4-one
Reaction equation
CN(C)/[CH:3]=[CH:4]/[C:5]([C:7]1[C:12](=[O:13])[CH:11]=[CH:10][N:9]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([S:20]([N:23]3[CH2:27][CH2:26][CH2:25][CH2:24]3)(=[O:22])=[O:21])[CH:15]=2)[N:8]=1)=O.[N:29]1[C:38]2[C:33](=[C:34]([NH:39][NH2:40])[CH:35]=[CH:36][CH:37]=2)[CH:32]=[CH:31][CH:30]=1>>[N:23]1([S:20]([C:16]2[CH:15]=[C:14]([N:9]3[CH:10]=[CH:11][C:12](=[O:13])[C:7]([C:5]4[N:39]([C:34]5[CH:35]=[CH:36][CH:37]=[C:38]6[C:33]=5[CH:32]=[CH:31][CH:30]=[N:29]6)[N:40]=[CH:3][CH:4]=4)=[N:8]3)[CH:19]=[CH:18][CH:17]=2)(=[O:22])=[O:21])[CH2:24][CH2:25][CH2:26][CH2:27]1Participants
3
Procedure
The product was obtained starting from 3-((E)-3-Dimethylamino-acryloyl)-1-[3-(pyrrolidine-1-sulfonyl)-phenyl]-1H-pyridazin-4-one (A-29) and quinolin-5-yl-hydrazine according to the method described for example 91. MS: M=499.2 (M+H)+
Workup
- customThe product was obtained
Sources & evidence
- ORD record
- ord-6f068b0bf51641229e2ac9682d62e836
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08178538B2
Reaction notes
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