3-Cyanobenzoyl chloride → HCID 68578606, compound

HRID 1443775Notes

Reaction equation

HRID 1443775 reaction equation
[N:1]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[NH:4][CH2:3][CH:2]2[C:10]1[CH:15]=[CH:14][C:13]([NH2:16])=[CH:12][CH:11]=1.[C:17]([C:19]1[CH:20]=[C:21]([CH:25]=[CH:26][CH:27]=1)[C:22]([Cl:24])=[O:23])#[N:18]>>[ClH:24].[N:1]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[NH:4][CH2:3][CH:2]2[C:10]1[CH:15]=[CH:14][C:13]([NH:16][C:22](=[O:23])[C:21]2[CH:25]=[CH:26][CH:27]=[C:19]([C:17]#[N:18])[CH:20]=2)=[CH:12][CH:11]=1

Participants

3

Reactant 2

HCID 3084833-Cyanobenzoyl chlorideHCID 68576408HCID 68576408, compound

Product 1

HCID 68578606HCID 68578606, compound

Procedure

Was prepared by Method G from 4-(1,4-diaza-bicyclo[3.2.2]non yl)-phenylamine and 3-cyanobenzoyl chloride. Mp. 250° C. (decomp.).

Sources & evidence

ORD record
ord-1ac689df5a6b46059e5f1d4295a0f5c1
Source dataset
uspto-grants-2010_02
Patent number
US07662808B2

Reaction notes

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