Piperidine → N-(2,6,10,14,18-pentamethyl-22-oxo-2,6,10,14,18-tricosapentaenoyl)piperidin

HRID 477621Notes

Reaction equation

[CH3:1][C:2](=[CH:6][CH2:7][CH2:8][C:9]([CH3:31])=[CH:10][CH2:11][CH2:12][C:13]([CH3:30])=[CH:14][CH2:15][CH2:16][C:17]([CH3:29])=[CH:18][CH2:19][CH2:20][C:21]([CH3:28])=[CH:22][CH2:23][CH2:24][C:25](=[O:27])[CH3:26])[C:3]([OH:5])=O.[NH:32]1[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]1>>[CH3:1][C:2](=[CH:6][CH2:7][CH2:8][C:9]([CH3:31])=[CH:10][CH2:11][CH2:12][C:13]([CH3:30])=[CH:14][CH2:15][CH2:16][C:17]([CH3:29])=[CH:18][CH2:19][CH2:20][C:21]([CH3:28])=[CH:22][CH2:23][CH2:24][C:25](=[O:27])[CH3:26])[C:3]([N:32]1[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]1)=[O:5]

Participants

Reactant 2

HCID 8082Piperidine

HCID 538735642,6,10,14,18-Pentamethyl-22-oxo-2,6,10,14,18-tricosapentaenoic acid

Product 1

HCID 54236937N-(2,6,10,14,18-pentamethyl-22-oxo-2,6,10,14,18-tricosapentaenoyl)piperidin

Procedure

Starting materials: 2,6,10,14,18-pentamethyl-22-oxo-2,6,10,14,18-tricosapentaenoic acid and piperidine.

Sources & evidence

ORD record: ord-c4b44eab8a8843b7b9abf31c0adf25d2
Source dataset: uspto-grants-1989_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04888439

Reaction notes

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