1-Benzyl-4-piperidone → HCID 20484284, compound

HRID 647930Notes

Reaction equation

HRID 647930 reaction equation
[NH:1]([C:3]1[CH:4]=[CH:5][C:6]2[S:10][CH:9]=[C:8]([CH3:11])[C:7]=2[CH:12]=1)N.[CH2:13]([N:20]1[CH2:25][CH2:24][C:23](=O)[CH2:22][CH2:21]1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[CH2:13]([N:20]1[CH2:25][CH2:24][C:23]2[NH:1][C:3]3[C:12]([C:22]=2[CH2:21]1)=[C:7]1[C:8]([CH3:11])=[CH:9][S:10][C:6]1=[CH:5][CH:4]=3)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

3

Reactant 2

HCID 192201-Benzyl-4-piperidoneHCID 12658438HCID 12658438, compound

Product 1

HCID 20484284HCID 20484284, compound

Procedure

The compound is formed analogously to the compound described in Example 5, from 10.1 g of 5-hydrazino-3-methylbenzothiophene and 10 ml of benzyl-4-piperidone. Melting point: 93° C.

Workup

  1. customThe compound is formed analogously to the compound

Sources & evidence

ORD record
ord-f3eab77dd2244fa08310cc751040f5d3
Source dataset
uspto-grants-1983_10
Patent number
US04410536

Reaction notes

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