4-Chlorobenzylamine → HCID 21498280, compound

HRID 1730512Notes

Reaction equation

HRID 1730512 reaction equation
[CH2:1]([CH:5]1[C:10](=O)[CH:9]([CH3:12])[CH2:8][N:7]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:6]1)[C:2]([CH3:4])=O.[Cl:20][C:21]1[CH:28]=[CH:27][C:24]([CH2:25][NH2:26])=[CH:23][CH:22]=1>>[CH2:13]([N:7]1[CH2:8][CH:9]([CH3:12])[C:10]2[N:26]([CH2:25][C:24]3[CH:27]=[CH:28][C:21]([Cl:20])=[CH:22][CH:23]=3)[C:2]([CH3:4])=[CH:1][C:5]=2[CH2:6]1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

3

Reactant 2

HCID 660364-ChlorobenzylamineHCID 21498268HCID 21498268, compound

Product 1

HCID 21498280HCID 21498280, compound

Procedure

Using a procedure analogous to Example 3, 3-acetonyl-1-benzyl-5-methyl-4-piperidone may be reacted with p-chlorobenzylamine to give the title compound.

Sources & evidence

ORD record
ord-d51993f60f8745458a903bebdd225a88
Source dataset
uspto-grants-1976_11
Patent number
US03992544

Reaction notes

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