3-Fluorobenzoyl chloride → HCID 68566441, compound
Reaction equation
[N:1]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[N:4]([C:10]1[CH:15]=[CH:14][C:13]([NH2:16])=[CH:12][CH:11]=1)[CH2:3][CH2:2]2.[F:17][C:18]1[CH:19]=[C:20]([CH:24]=[CH:25][CH:26]=1)[C:21]([Cl:23])=[O:22]>>[ClH:23].[N:1]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[N:4]([C:10]1[CH:15]=[CH:14][C:13]([NH:16][C:21](=[O:22])[C:20]3[CH:24]=[CH:25][CH:26]=[C:18]([F:17])[CH:19]=3)=[CH:12][CH:11]=1)[CH2:3][CH2:2]2Participants
3
Procedure
Was prepared by Method G from 4-(1,4-diaza-bicyclo[3.2.2]non-4-yl)-phenylamine and 3-fluorobenzoyl chloride. Mp. >270° C. (decomp.).
Sources & evidence
- ORD record
- ord-89b81854294e4c2a9a276d3065303e75
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08236793B2
Reaction notes
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