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

Sulfoxonium, trimethyl-, iodide (1:1) → 5-(1-Phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-carboxylic acid

HRID 1177402
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1177402
[CH3:1]C([O-])(C)C.[K+].[I-].C[S+](C)(C)=O.[C:13]1([C:19]([C:21]2[N:26]=[C:25]3[S:27][C:28]([C:30]([O-:32])=[O:31])=[N:29][C:24]3=[CH:23][CH:22]=2)=[CH2:20])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[Na+]>CS(C)=O.Cl>[C:13]1([C:19]2([C:21]3[N:26]=[C:25]4[S:27][C:28]([C:30]([OH:32])=[O:31])=[N:29][C:24]4=[CH:23][CH:22]=3)[CH2:1][CH2:20]2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 74498Sulfoxonium, trimethyl-, iodide (1:1)HCID 23665647Potassium tert-butoxideHCID 67111612HCID 67111612, Verbindung

Produkt 1

HCID 671116745-(1-Phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 313Hydrochloric AcidLösungsmittel
HCID 679
Dimethyl Sulfoxide
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

Potassium 2-methylpropan-2-olate (0.66 g, 5.9 mmol) was dissolved in anhydrous DMSO (19.5 mL) under argon. Trimethylsulfoxonium iodide (1.3 g, 5.9 mmol) was added to the resulting solution in one portion. After 10 min, this dissolved, and the resulting clear solution was added via cannula (over ˜2 min) to a suspension of sodium 5-(1-phenylvinyl)thiazolo[5,4-b]pyridine-2-carboxylate (1.19 g, 3.9 mmol) in DMSO (5 mL) at 25° C. The resulting solution was stirred at 25° C. for 1 h. The reaction solution was then diluted with 1.0N HCl (8.0 mL) and partitioned between dichloromethane (400 mL) and water (400 mL). The organic layer was separated, and the aqueous layer was extracted with additional dichloromethane (200 mL). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated in vacuo to afford crude 5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-carboxylic acid as a yellow oil. MS (ESI) m/z: Calculated: 296.1; Observed: 297.0 (M++1).

Aufarbeitung

  1. custompartitioned between dichloromethane (400 mL) and water (400 mL)
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was extracted with additional dichloromethane (200 mL)
  4. dry with materialThe combined organic extracts were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-ceafd9b22cc747369880d343e9111e9d
Quelldatensatz
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07842685B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion