4-(N-Propionylaniline)piperidine → HCID 131710806, compound

HRID 2399174Notes

Reaction equation

HRID 2399174 reaction equation
[C:1]1([O:11][CH:12](Br)[CH3:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[C:15]1([N:21]([CH:26]2[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]2)[C:22](=[O:25])[CH2:23][CH3:24])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C1CCCCC1>[C:1]1([O:11][CH:12]([N:29]2[CH2:28][CH2:27][CH:26]([N:21]([C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:22](=[O:25])[CH2:23][CH3:24])[CH2:31][CH2:30]2)[CH3:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1

Participants

4

Reactant 2

HCID 2593814-(N-Propionylaniline)piperidineHCID 131710807HCID 131710807, compound

Product 1

HCID 131710806HCID 131710806, compound

Reagents, catalysts & solvents 1

HCID 8078CyclohexaneSolvent

Procedure

Using the procedure of Example I step B and starting from (α-naphtoxyethyl) bromide and 4(N-phenyl N-propionylamino) piperidine, N(α-naphtoxyethyl) 4-(N'-phenyl-N'-propionylamino) piperidine is obtained melting at 110°-112° (cyclohexane).

Sources & evidence

ORD record
ord-89b4f108da6a46ab9c380e5711fa6c74
Source dataset
uspto-grants-1977_05
Patent number
US04027028

Reaction notes

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