4-Piperidinecarboxamide → HCID 18678656, compound

HRID 1634780Notes

Reaction equation

[NH:1]1[CH2:9][CH2:8][CH:4]([C:5]([NH2:7])=[O:6])[CH2:3][CH2:2]1.Br[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].C(=O)([O-])[O-].[K+].[K+]>>[CH2:25]([N:1]1[CH2:9][CH2:8][CH:4]([C:5]([NH2:7])=[O:6])[CH2:3][CH2:2]1)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH3:11]

Participants

Reactant 3

HCID 37724-Piperidinecarboxamide

HCID 11430Potassium Carbonate

HCID 123941-Bromopentadecane

Product 1

HCID 18678656HCID 18678656, compoundYield 85.2%

Procedure

Prepared from isonipecotamide (2.0 g, 15.6 mmol), 1-bromopentadecane (4.5 g, 15.6 mmol) and potassium carbonate (2.16 g, 15.6 mmol) according to procedure used for Example 8 (Step A) to give 4.5 g of the title compound as a white solid.

Sources & evidence

ORD record: ord-129c849db5df4ceca8d4b719f1ee8043
Source dataset: uspto-grants-2003_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06506901B2

Reaction notes

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