Iodoethane → HCID 66998278, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[C:28](=[O:29])[N:27]([CH3:30])[C:12]2[N:13]([CH3:26])[C:14]3[C:19]([C:11]=2[CH:10]=1)=[CH:18][C:17]([C:20]1[NH:24][N:23]=[C:22]([CH3:25])[CH:21]=1)=[CH:16][CH:15]=3.I[CH2:32][CH3:33]>>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[C:28](=[O:29])[N:27]([CH3:30])[C:12]2[N:13]([CH3:26])[C:14]3[C:19]([C:11]=2[CH:10]=1)=[CH:18][C:17]([C:20]1[CH:21]=[C:22]([CH3:25])[N:23]([CH2:32][CH3:33])[N:24]=1)=[CH:16][CH:15]=3Participants
3
Procedure
The process is carried out as indicated in Example 36 above, using 3-(2,4-dichlorophenyl)-1,9-dimethyl-6-(3-methyl-1H-pyrazol-5-yl)-1,9-dihydro-2H-pyrido[2,3-b]indol-2-one described in Example 46 above and iodoethane.
Sources & evidence
- ORD record
- ord-91ad07bd075a4847b3aaf73a86e3458d
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08063061B2
Reaction notes
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