4-Nitrobenzoyl chloride → HCID 68563876, compound

HRID 882729Notes

Reaction equation

HRID 882729 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:28]=[CH:27][C:23]([C:24]([Cl:26])=[O:25])=[CH:22][CH:21]=1)([O-:19])=[O:18]>>[ClH:26].[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:24](=[O:25])[C:23]3[CH:22]=[CH:21][C:20]([N+:17]([O-:19])=[O:18])=[CH:28][CH:27]=3)=[CH:12][CH:11]=1)[CH2:3][CH2:2]2

Participants

3

Reactant 2

HCID 85024-Nitrobenzoyl chlorideHCID 67441600HCID 67441600, compound

Product 1

HCID 68563876HCID 68563876, compound

Procedure

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

Sources & evidence

ORD record
ord-c6ab91deaad240dfb3c876796a7b3b5c
Source dataset
uspto-grants-2012_08
Patent number
US08236793B2

Reaction notes

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