1-Chloro-4-nitronaphthalene → HCID 10804994, compound

HRID 1647727Notes

Reaction equation

HRID 1647727 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([N+:12]([O-:14])=[O:13])=[CH:4][CH:3]=1.[N:15]12[CH2:22][CH2:21][CH2:20][C:19]1([CH2:23][NH2:24])[CH2:18][CH2:17][CH2:16]2>>[N:15]12[CH2:22][CH2:21][CH2:20][C:19]1([CH2:23][NH:24][C:2]1[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]([N+:12]([O-:14])=[O:13])=[CH:4][CH:3]=1)[CH2:18][CH2:17][CH2:16]2

Participants

3

Reactant 2

HCID 3127191-Chloro-4-nitronaphthaleneHCID 10654304(Hexahydro-1H-pyrrolizin-7A-YL)methanamine

Product 1

HCID 10804994HCID 10804994, compoundYield 50.9%

Procedure

1-Chloro-4-nitronaphthalene and (1-azabicyclo[3.3.0]octan-5-yl)methylamine were reacted in the same manner as in Example 1 to obtain the titled compound in a yield of 50.9%.

Sources & evidence

ORD record
ord-cbd387920e2041b691369b194dff57d3
Source dataset
uspto-grants-1995_07
Patent number
US05434165

Reaction notes

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