4-Fluorobenzoyl chloride → HCID 67095875, compound
Reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[NH2:15][C@H:16]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:18][CH2:17]1.[F:25][C:26]1[CH:34]=[CH:33][C:29]([C:30](Cl)=[O:31])=[CH:28][CH:27]=1>>[F:25][C:26]1[CH:34]=[CH:33][C:29]([C:30]([NH:1][C:4]2[CH:13]=[CH:12][CH:11]=[C:10]3[C:5]=2[CH:6]=[CH:7][C:8]([NH:15][C@H:16]2[C:24]4[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=4)[CH2:18][CH2:17]2)=[N:9]3)=[O:31])=[CH:28][CH:27]=1Participants
4
Procedure
The title compound, MS: m/e=398.1 (M+H+), was prepared in accordance with the general method of example 45 from 5-nitro-2-chloroquinoline, (R)-1-aminoindane and 4-fluorobenzoyl chloride.
Sources & evidence
- ORD record
- ord-bcd2a2f5a81e4bd990dd61d9df23efb9
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07923561B2
Reaction notes
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