1-(Prop-2-yn-1-yl)piperidine → HCID 15390917, compound

HRID 1738798Notes

Reaction equation

HRID 1738798 reaction equation
[CH2:1]([N:5]1[C:13]2[N:12]=[CH:11][N:10]([CH2:14][CH2:15][CH3:16])[C:9]=2[C:8](=[O:17])[N:7]([CH2:18][CH2:19][CH2:20][CH2:21][C:22](=[O:24])[CH3:23])[C:6]1=[O:25])[CH2:2][CH2:3][CH3:4].[CH2:26]([N:29]1[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1)[C:27]#[CH:28]>>[CH2:1]([N:5]1[C:13]2[N:12]=[CH:11][N:10]([CH2:14][CH2:15][CH3:16])[C:9]=2[C:8](=[O:17])[N:7]([CH2:18][CH2:19][CH2:20][CH2:21][C:22]([OH:24])([CH3:23])[C:28]#[C:27][CH2:26][N:29]2[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]2)[C:6]1=[O:25])[CH2:2][CH2:3][CH3:4]

Participants

3

Reactant 2

HCID 3366521-(Prop-2-yn-1-yl)piperidineHCID 15390929HCID 15390929, compound

Product 1

HCID 15390917HCID 15390917, compoundYield 58%

Procedure

The compound was prepared as oily substance in 58% yield using 3-butyl-1-(5-oxohexyl)-7-propylxanthine and N-(2-propynyl)piperidine as in Example 6C1).

Workup

  1. customThe compound was prepared as oily substance in 58% yield

Sources & evidence

ORD record
ord-ce62cb7122e24891bcc9d759fd2e93e5
Source dataset
uspto-grants-1999_10
Patent number
US05965555

Reaction notes

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