HCID 19888357, compound → HCID 19888359, compound

HRID 654086Notes

Reaction equation

HRID 654086 reaction equation
[N+:1]([C:4]1[CH:24]=[CH:23][C:7]([O:8][CH2:9][CH2:10][CH:11]2[CH2:14][N:13]([CH:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH3:16])[CH2:12]2)=[CH:6][CH:5]=1)([O-])=O>[Pt].C(O)C>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([O:8][CH2:9][CH2:10][CH:11]2[CH2:12][N:13]([CH:15]([C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH3:16])[CH2:14]2)=[CH:23][CH:24]=1

Participants

4

Reactant 1

HCID 19888357HCID 19888357, compound

Product 1

HCID 19888359HCID 19888359, compound

Reagents, catalysts & solvents 2

HCID 23939PlatinumCatalystHCID 702EthanolSolvent

Procedure

The title compound is prepared by catalytic reduction at room temperature in the presence of platinum on carbon catalyst in ethanol solution using standard laboratory procedures from 3-[2-(4-nitrophenoxy)ethyl]-1-(1-phenylethyl)azetidine.

Sources & evidence

ORD record
ord-de5063ed57e346b986762f648046b404
Source dataset
uspto-grants-1992_07
Patent number
US05130309

Reaction notes

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