Benzoyl chloride, 3-nitro- → HCID 68566514, compound
Reaction equation
[N:1]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[N:4]([C:10]1[N:15]=[CH:14][C:13]([NH2:16])=[CH:12][CH:11]=1)[CH2:3][CH2:2]2.[N+:17]([C:20]1[CH:21]=[C:22]([CH:26]=[CH:27][CH:28]=1)[C:23]([Cl:25])=[O:24])([O-:19])=[O:18]>>[ClH:25].[N:1]12[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9]1)[N:4]([C:10]1[N:15]=[CH:14][C:13]([NH:16][C:23](=[O:24])[C:22]3[CH:26]=[CH:27][CH:28]=[C:20]([N+:17]([O-:19])=[O:18])[CH:21]=3)=[CH:12][CH:11]=1)[CH2:3][CH2:2]2Participants
3
Procedure
Was prepared according to Method G from 6-(1,4-diaza-bicyclo[3.2.2]non-4-yl)-pyridin-3-ylamine and 3-nitrobenzoyl chloride. Mp. >280° C. (decomp.).
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-0c4f6adfeeb14ef1a3b7609ba4c7b970
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08236793B2
Reaction notes
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