Iodoethane → HCID 66998822, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:26](=[O:27])[N:25]([CH3:28])[C:11]3[N:12]([CH3:24])[C:13]4[C:18]([C:10]=3[CH:9]=2)=[CH:17][C:16]([C:19]2[NH:20][N:21]=[CH:22][CH:23]=2)=[CH:15][CH:14]=4)=[CH:4][CH:3]=1.I[CH2:30][CH3:31]>>[CH2:30]([N:21]1[CH:22]=[CH:23][C:19]([C:16]2[CH:17]=[C:18]3[C:13](=[CH:14][CH:15]=2)[N:12]([CH3:24])[C:11]2[N:25]([CH3:28])[C:26](=[O:27])[C:8]([C:5]4[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=4)=[CH:9][C:10]3=2)=[N:20]1)[CH3:31]Participants
3
Procedure
The process is carried out as indicated in Example 36 above, with the compound from Example 72, 3-(4-fluorophenyl)-1,9-dimethyl-6-(2H-pyrazol-3-yl)-1,9-dihydropyrido[2,3-b]indol-2-one and iodoethane.
Sources & evidence
- ORD record
- ord-401177df86ec4aaca26075d149f92247
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08063061B2
Reaction notes
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