3-Cyanobenzoyl chloride → HCID 68567830, compound

HRID 882741Notes

Reaction equation

HRID 882741 reaction equation
[N:1]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[N:4]([C:10]1[N:15]=[CH:14][C:13]([NH2:16])=[CH:12][CH:11]=1)[CH2:3][CH2:2]2.[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[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9]1)[N:4]([C:10]1[N:15]=[CH:14][C:13]([NH:16][C:22](=[O:23])[C:21]3[CH:25]=[CH:26][CH:27]=[C:19]([C:17]#[N:18])[CH:20]=3)=[CH:12][CH:11]=1)[CH2:3][CH2:2]2

Participants

3

Reactant 2

HCID 3084833-Cyanobenzoyl chlorideHCID 68565532HCID 68565532, compound

Product 1

HCID 68567830HCID 68567830, compound

Procedure

Was prepared according to Method G from 6-(1,4-diaza-bicyclo[3.2.2]non-4-yl)-pyridin-3-ylamine and 3-cyanobenzoyl chloride. Mp. >265° C. (decomp.).

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-9818da0d29894bfdbe76e4eda0b6c0a0
Source dataset
uspto-grants-2012_08
Patent number
US08236793B2

Reaction notes

Loading…