StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Methyl iodide → HCID 66973304, Verbindung

HRID 1864870
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1864870
C[Si]([N-][Si](C)(C)C)(C)C.[Na+].[CH2:11]1COCC1.[F:16][C:17]1[CH:18]=[C:19]([C@@H:24]2[CH2:29][CH2:28][CH2:27][C:26](=[O:30])[N:25]2[C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[CH:20]=[C:21]([F:23])[CH:22]=1.IC>COCCOC>[F:16][C:17]1[CH:18]=[C:19]([C@H:24]2[N:25]([C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[C:26](=[O:30])[C@H:27]([CH3:11])[CH2:28][CH2:29]2)[CH:20]=[C:21]([F:23])[CH:22]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6328Methyl iodideHCID 8028TetrahydrofuranHCID 2724254Sodium bis(trimethylsilyl)amideHCID 66865136HCID 66865136, Verbindung2×

Produkt 1

HCID 66973304HCID 66973304, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8071
1,2-Dimethoxyethane
Lösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a 1 M solution of sodium bis(trimethylsilyl)amide in THF (0.642 mL, 0.642 mmol) at −78° C. was added dropwise a solution of tert-butyl (2S)-2-(3,5-difluorophenyl)-6-oxopiperidine-1-carboxylate (200 mg, 0.642 mmol, described in Intermediate 26) in DME (10 mL) at −78° C. The resulting mixture was stirred at −78° C. for 10 min then iodomethane (0.040 mL, 0.642 mmol) was added. After stirring at −78° C. for 30 min and at −30° C. for 30 min, the reaction mixture was cooled to −78° C. and quenched with saturated aqueous NH4Cl (10 mL) and extracted with EtOAc (2×10 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc-100:0 to 90:10. MS: m/z=270 (M−C4H7).

Aufarbeitung

  1. stirringAfter stirring at −78° C. for 30 min and at −30° C. for 30 min
  2. temperaturethe reaction mixture was cooled to −78° C.
  3. customquenched with saturated aqueous NH4Cl (10 mL)
  4. extractionextracted with EtOAc (2×10 mL)
  5. dry with materialThe combined organic layers were dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe crude product was purified by silica gel chromatography
  9. washeluting with a gradient of hexane

Quellen und Nachweise

ORD-Eintrag
ord-65918b507de949cc83300a388d24fde2
Quelldatensatz
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07625901B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion