Piperidine → HCID 66738754, Verbindung

HRID 229333

Reaktionsgleichung

Reaktionsgleichung von HRID 229333
[C:1](#[N:10])[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:11][C:12]1[NH:16][N:15]=[C:14]([NH2:17])[CH:13]=1.[NH:18]1[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1>>[CH3:11][C:12]1[NH:16][N:15]=[C:14]([NH:17][C:3]2[CH:2]=[C:1]([N:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)[N:10]=[C:1]([CH:2]=[CH:3][C:4]3[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=3)[N:10]=2)[CH:13]=1

Komponenten

4

Edukt 3

HCID 8082PiperidineHCID 746673-Phenylprop-2-enenitrileHCID 931461H-Pyrazol-3-amine, 5-methyl-

Produkt 1

HCID 66738754HCID 66738754, Verbindung

Versuchsvorschrift

Example 67 was synthesized via Scheme 6 according to the general scheme provided above with the appropriate starting materials cinnamonitrile, 5-methyl-1H-pyrazole-3-amine, and piperidine. Structure of the target was confirmed by 1H-NMR. The 1H-NMR is attached.

Aufarbeitung

  1. customExample 67 was synthesized via Scheme 6 according to the general scheme
  2. customprovided above with the

Quellen und Nachweise

ORD-Eintrag
ord-3ab779a86c914edb8b72ac741e21483b
Quelldatensatz
uspto-grants-2009_07
Patentnummer
US07563787B2

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