Pyridine → (S)-N-(3-(1-ethyl-1H-pyrazol-5-yloxy)-5-(pyridin-2-ylthio)pyridin-2-yl)-3-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)-1,2,4-thiadiazol-5-amine

HRID 1523602Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1523602
[N-:1]=[C:2]=[S:3].[Na+].N1C=CC=CC=1.[CH3:11][C:12]1([CH3:27])[O:16][C@@H:15]([C:17](Cl)=[N:18]OS(C)(=O)=O)[C:14]([CH3:26])([CH3:25])[O:13]1.[CH2:28]([N:30]1[C:34]([O:35][C:36]2[C:37]([NH2:49])=[N:38][CH:39]=[C:40]([S:42][C:43]3[CH:48]=[CH:47][CH:46]=[CH:45][N:44]=3)[CH:41]=2)=[CH:33][CH:32]=[N:31]1)[CH3:29]>CCOC(C)=O.[OH-].[Na+]>[CH2:28]([N:30]1[C:34]([O:35][C:36]2[C:37]([NH:49][C:2]3[S:3][N:18]=[C:17]([C@H:15]4[C:14]([CH3:25])([CH3:26])[O:13][C:12]([CH3:11])([CH3:27])[O:16]4)[N:1]=3)=[N:38][CH:39]=[C:40]([S:42][C:43]3[CH:48]=[CH:47][CH:46]=[CH:45][N:44]=3)[CH:41]=2)=[CH:33][CH:32]=[N:31]1)[CH3:29]

Komponenten

7

Edukt 4

HCID 1049PyridineHCID 10953423IsothiocyanatosodiumHCID 674860483-(1-ethyl-1H-pyrazol-5-yloxy)-5-(pyridin-2-ylthio)pyridin-2-amineHCID 86644154(R)-2,2,5,5-tetramethyl-N-(methylsulfonyloxy)-1,3-dioxolane-4-carbimidoyl chloride

Produkt 1

HCID 68476855(S)-N-(3-(1-ethyl-1H-pyrazol-5-yloxy)-5-(pyridin-2-ylthio)pyridin-2-yl)-3-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)-1,2,4-thiadiazol-5-amineAusbeute 32 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8857Ethyl AcetateLösungsmittel2×HCID 14798Sodium HydroxideLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To 30 mL of EtOAc was added sodium isothiocyanate (0.0970 g, 1.20 mmol), pyridine (0.195 ml, 2.39 mmol) and (R)-2,2,5,5-tetramethyl-N-(methylsulfonyloxy)-1,3-dioxolane-4-carbimidoyl chloride (0.342 g, 1.20 mmol). The reaction was heated to 60° C. for 15 minutes. To the mixture was added 3-(1-ethyl-1H-pyrazol-5-yloxy)-5-(pyridin-2-ylthio)pyridin-2-amine (0.250 g, 0.798 mmol) and the reaction was stirred overnight at 70° C. The reaction was cooled and diluted with 50 ml EtOAc and 50 ml 1N NaOH. The aqueous layer was extracted with EtOAc. The combined organic layers were dried over Na2SO4, filtered and concentrated in-vacuo. The residue was purified over silica gel (50% EtOAc/Hexanes) to afford (S)—N-(3-(1-ethyl-1H-pyrazol-5-yloxy)-5-(pyridin-2-ylthio)pyridin-2-yl)-3-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)-1,2,4-thiadiazol-5-amine (0.134 g, 0.255 mmol, 32.0% yield).

Aufarbeitung

  1. temperatureThe reaction was cooled
  2. extractionThe aqueous layer was extracted with EtOAc
  3. dry with materialThe combined organic layers were dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated in-vacuo
  6. customThe residue was purified over silica gel (50% EtOAc/Hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-a4574630cc01473a9f763b38eeb7926d
Quelldatensatz
uspto-grants-2015_07
Patentnummer
US09079890B2

Notizen zur Reaktion

Wird geladen…