4-Cyanobenzoyl chloride → HCID 68565717, compound

HRID 882734Notes

Reaction equation

HRID 882734 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.[C:17]([C:19]1[CH:27]=[CH:26][C:22]([C:23]([Cl:25])=[O:24])=[CH:21][CH:20]=1)#[N: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][C:19]([C:17]#[N:18])=[CH:20][CH:21]=3)=[CH:12][CH:11]=1)[CH2:3][CH2:2]2

Participants

3

Reactant 2

HCID 801724-Cyanobenzoyl chlorideHCID 67441600HCID 67441600, compound

Product 1

HCID 68565717HCID 68565717, compound

Procedure

Was prepared by Method G from 4-(1,4-diaza-bicyclo[3.2.2]non-4-yl)-phenylamine and 4-cyanobenzoyl chloride. Mp. 250° C. (decomp.).

Sources & evidence

ORD record
ord-f1889b41204f41ccbba92e8d7ecbe69c
Source dataset
uspto-grants-2012_08
Patent number
US08236793B2

Reaction notes

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