tert-Butoxy bis(dimethylamino)methane → HCID 66997540, compound
Reaction equation
[C:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9]([CH3:13])[C:8]1[N:14]([CH3:27])[C:15](=[O:26])[C:16]([C:18]3[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][C:19]=3[F:25])=[CH:17][C:7]2=1)(=[O:3])[CH3:2].CC(O[CH:33](N(C)C)[N:34]([CH3:36])[CH3:35])(C)C>>[Cl:24][C:21]1[CH:22]=[CH:23][C:18]([C:16]2[C:15](=[O:26])[N:14]([CH3:27])[C:8]3[N:9]([CH3:13])[C:10]4[C:6]([C:7]=3[CH:17]=2)=[CH:5][C:4]([C:1](=[O:3])[CH:2]=[CH:33][N:34]([CH3:36])[CH3:35])=[CH:12][CH:11]=4)=[C:19]([F:25])[CH:20]=1Participants
3
Procedure
The process is carried out as indicated in preparation 1.9C above, with compound B 6-acetyl-3-(4-chloro-2-fluorophenyl)-1,9-dimethyl-1,9-dihydropyrido[2,3-b]indol-2-one and Bredereck's reagent.
Sources & evidence
- ORD record
- ord-c0b901a9537648c9974835aefe836396
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08063061B2
Reaction notes
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