3-(Pyridin-3-yl)propan-1-amine → HCID 178482569, compound

HRID 1090246Notes

Reaction equation

HRID 1090246 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][CH2:8][CH2:9][NH2:10])[CH:2]=1.[CH3:11][N:12]([CH3:26])[C:13]1[CH:14]=[C:15]2[CH:23]=[CH:22][CH:21]=[C:20]3[C:16]2=[C:17]([CH:25]=1)[C:18](S)=[N:19]3>C(O)C>[CH3:11][N:12]([CH3:26])[C:13]1[CH:14]=[C:15]2[CH:23]=[CH:22][CH:21]=[C:20]3[C:16]2=[C:17]([CH:25]=1)[C:18]([NH:10][CH2:9][CH2:8][CH2:7][C:3]1[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=1)=[N:19]3

Participants

4

Reactant 2

HCID 135575233-(Pyridin-3-yl)propan-1-amineHCID 178482570HCID 178482570, compound

Product 1

HCID 178482569HCID 178482569, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

The reaction of equivalent molar quantities of 3-(3-pyridinyl)propanamine, 4-dimethylaminobenz(cd)indol-2thiol, and mercuric acetate in refluxing ethanol, under the conditions of Example 55 leads to the formation of the title compound.

Sources & evidence

ORD record
ord-a46d626d025647338c2c67326a279c66
Source dataset
uspto-grants-1992_01
Patent number
US05081131

Reaction notes

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