Benzoyl chloride, 3-nitro- → HCID 68565417, compound

HRID 882728Notes

Reaction equation

HRID 882728 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.[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[CH2:9][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][CH:28]=[C:20]([N+:17]([O-:19])=[O:18])[CH:21]=3)=[CH:12][CH:11]=1)[CH2:3][CH2:2]2

Participants

3

Reactant 2

HCID 8495Benzoyl chloride, 3-nitro-HCID 67441600HCID 67441600, compound

Product 1

HCID 68565417HCID 68565417, compound

Procedure

Was prepared by Method G from 4-(1,4-Diaza-bicyclo[3.2.2]non-4-yl)-phenylamine and 3-nitrobenzoyl chloride. Mp. >280° C.

Sources & evidence

ORD record
ord-736219bf5b494695bd967aeae8c13722
Source dataset
uspto-grants-2012_08
Patent number
US08236793B2

Reaction notes

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