4-[3-(Dimethylamino)-1-propyn-1-yl]benzenamine → HCID 178483389, compound
Reaction equation
C(O[C:4](=[C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=2)[NH:13][C:12]1=[O:23])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)C.[CH3:24][N:25]([CH3:36])[CH2:26][C:27]#[C:28][C:29]1[CH:35]=[CH:34][C:32]([NH2:33])=[CH:31][CH:30]=1>>[CH3:36][N:25]([CH3:24])[CH2:26][C:27]#[C:28][C:29]1[CH:30]=[CH:31][C:32]([NH:33]/[C:4](=[C:11]2\[C:12](=[O:23])[NH:13][C:14]3[C:19]\2=[CH:18][C:17]([N+:20]([O-:22])=[O:21])=[CH:16][CH:15]=3)/[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)=[CH:34][CH:35]=1Participants
3
Procedure
Prepared analogously to Example 89 by reacting 3-(1-ethoxy-1-phenyl-methylidene)-5-nitro-2-indolinone with 4-(3-dimethylaminoprop-1-ynyl)-aniline.
Workup
- customPrepared analogously to Example 89
Sources & evidence
- ORD record
- ord-270607f06ed94c1695df3da516483c30
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06855710B2
Reaction notes
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