p-Anisoyl chloride → HCID 68563706, compound

HRID 882732Notes

Reaction equation

HRID 882732 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.[CH3:17][O:18][C:19]1[CH:27]=[CH:26][C:22]([C:23]([Cl:25])=[O:24])=[CH:21][CH:20]=1>>[ClH:25].[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:23](=[O:24])[C:22]3[CH:26]=[CH:27][C:19]([O:18][CH3:17])=[CH:20][CH:21]=3)=[CH:12][CH:11]=1)[CH2:3][CH2:2]2

Participants

3

Reactant 2

HCID 7477p-Anisoyl chlorideHCID 67441600HCID 67441600, compound

Product 1

HCID 68563706HCID 68563706, compound

Procedure

Was prepared by Method G from 4-(1,4-diaza-bicyclo[3.2.2]non-4-yl)-phenylamine and 4-methoxybenzoyl chloride. Mp. >275° C.

Sources & evidence

ORD record
ord-a6f9e0d7ea304542aa479735f02342ea
Source dataset
uspto-grants-2012_08
Patent number
US08236793B2

Reaction notes

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