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Hydrochloric Acid → (NE,R)-N-[[5-[(2-fluorophenyl)methoxy]-2-pyridinyl]methylidene]-2-methylpropane-2-sulfinamide

HRID 511825
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 511825
[F:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[CH2:4][O:5][C:6]1[CH:7]=[CH:8][C:9]([C:12]#[N:13])=[N:10][CH:11]=1.CC(C[AlH]CC(C)C)C.Cl.C(=O)(O)[O-].[Na+].[CH3:33][C:34]([S@:37](N)=[O:38])([CH3:36])[CH3:35]>ClCCl.S([O-])([O-])(=O)=O.[Cu+2].CO>[F:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[CH2:4][O:5][C:6]1[CH:7]=[CH:8][C:9](/[CH:12]=[N:13]/[S@@:37]([C:34]([CH3:36])([CH3:35])[CH3:33])=[O:38])=[N:10][CH:11]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 5

HCID 313Hydrochloric AcidHCID 14487Diisobutylaluminum hydrideHCID 516892Sodium BicarbonateHCID 10964479tert-Butylsulfinamide, (R)-(+)-HCID 67290985HCID 67290985, Verbindung

Produkt 1

HCID 87457872(NE,R)-N-[[5-[(2-fluorophenyl)methoxy]-2-pyridinyl]methylidene]-2-methylpropane-2-sulfinamide
Ausbeute 36 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 24462Copper SulfateKatalysatorHCID 887MethanolLösungsmittelHCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a solution of Reactant 5-(2-fluorobenzyloxy)picolinonitrile (690 mg, 3.0 mmol) in dichloromethane (20 mL) was added DIBAL-H (3.7 mL, 3.6 mmol, 0.99 M) at −78° C. After being stirred at −78° C. for 4 hours, methanol (2 mL) was added to the mixture. 1N hydrochloric acid (0.5 mL) was added to the mixture at room temperature. The mixture was stirred at room temperature for 1 hour. Sat. sodium bicarbonate aqueous solution was added to the mixture until the pH was neutrized. The organic layer was extracted with dichloromethane, dried over sodium sulfate and concentrated in vacuo. The residue was dissolved in dichloromethane (20 mL). Copper(II) sulfate (1.2 g, 7.6 mmol) followed by (R)-(+)-2-methyl-2-propanesulfinamide (370 mg, 3.0 mmol) were added to the mixture respectively and the mixture was stirred for overnight at room temperature. The reaction mixture was filtrated off through a pad of Celite and the filtrate was concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with hexane/ethyl acetate (2:1 (v/v)) to give 360 mg (36% yield) of the title compound as a colorless oil:

Aufarbeitung

  1. stirringThe mixture was stirred at room temperature for 1 hour
  2. extractionThe organic layer was extracted with dichloromethane
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. dissolutionThe residue was dissolved in dichloromethane (20 mL)
  6. additionwere added to the mixture respectively
  7. stirringthe mixture was stirred for overnight at room temperature
  8. filtrationThe reaction mixture was filtrated off through a pad of Celite
  9. concentrationthe filtrate was concentrated in vacuo
  10. customThe residue was purified by column chromatography on silica gel eluting with hexane/ethyl acetate (2:1 (v/v))

Quellen und Nachweise

ORD-Eintrag
ord-f07bac2f0bbe4f6ca873d9d81206f310
Quelldatensatz
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09101616B2

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