(Hexahydro-1H-pyrrolizin-7A-YL)methanamine → HCID 10662828, compound

HRID 1647728Notes

Reaction equation

HRID 1647728 reaction equation
C(O[C:4]1[CH:13]=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]=1[N+:14]([O-:16])=[O:15])C.[N:17]12[CH2:24][CH2:23][CH2:22][C:21]1([CH2:25][NH2:26])[CH2:20][CH2:19][CH2:18]2>>[N:17]12[CH2:24][CH2:23][CH2:22][C:21]1([CH2:25][NH:26][C:4]1[CH:13]=[CH:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=1[N+:14]([O-:16])=[O:15])[CH2:20][CH2:19][CH2:18]2

Participants

3

Reactant 2

HCID 10654304(Hexahydro-1H-pyrrolizin-7A-YL)methanamineHCID 131627362-Ethoxy-1-nitronaphthalene

Product 1

HCID 10662828HCID 10662828, compoundYield 39.1%

Procedure

2-Ethoxy-1-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 39.1%.

Sources & evidence

ORD record
ord-c8ce4714959547aea82d8d2bc89ee7a5
Source dataset
uspto-grants-1995_07
Patent number
US05434165

Reaction notes

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