m-Anisoyl chloride → HCID 68565710, compound

HRID 882730Notes

Reaction equation

HRID 882730 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:20]=[C:21]([CH:25]=[CH:26][CH:27]=1)[C:22]([Cl:24])=[O:23]>>[ClH:24].[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: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]2

Participants

3

Reactant 2

HCID 74374m-Anisoyl chlorideHCID 67441600HCID 67441600, compound

Product 1

HCID 68565710HCID 68565710, compound

Procedure

Was prepared by Method G from 4-(1,4-diaza-bicyclo[3.2.2]non-4-yl)-phenylamine and 3-methoxybenzoyl chloride. Mp. 260° C.

Sources & evidence

ORD record
ord-e5693ec927b046ebb682dc0627be88f4
Source dataset
uspto-grants-2012_08
Patent number
US08236793B2

Reaction notes

Loading…