2-Nitrobenzoyl chloride → HCID 68565683, compound

HRID 1443771Notes

Reaction equation

HRID 1443771 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][CH:26]=[CH:25][C:21]=1[C:22]([Cl:24])=[O:23])([O-:19])=[O:18]>>[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]=[CH:28][C:20]=3[N+:17]([O-:19])=[O:18])=[CH:12][CH:11]=1)[CH2:3][CH2:2]2

Participants

3

Reactant 2

HCID 118752-Nitrobenzoyl chlorideHCID 67441600HCID 67441600, compound

Product 1

HCID 68565683HCID 68565683, compound

Procedure

Was prepared by Method G from 4-(1,4-Diaza-bicyclo[3.2.2]non-4-yl)phenylamine and 2-nitrobenzoyl chloride. Mp. >280° C.

Sources & evidence

ORD record
ord-c0456b27c3e940f488ea73d0074ddb33
Source dataset
uspto-grants-2010_02
Patent number
US07662808B2

Reaction notes

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