m-Anisoyl chloride → HCID 68562484, 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.[CH3:17][O:18][C:19]1[CH:20]=[C:21]([CH:25]=[CH:26][CH:27]=1)[C:22]([Cl:24])=[O:23]>>[ClH:24].[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:22](=[O:23])[C:21]3[CH:25]=[CH:26][CH:27]=[C:19]([O:18][CH3:17])[CH:20]=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-methoxybenzoyl chloride. Mp. >265° C. (decomp.).
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-d72f71fb684247aa8ba8ee0bef22ffd4
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662808B2
Reaction notes
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