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Dichloromethane → HCID 136117292, Verbindung

HRID 2204867
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2204867
Br[C:2]1[CH:7]=[CH:6][C:5]([S:8]([CH2:11][CH2:12][N:13]([CH3:15])[CH3:14])(=[O:10])=[O:9])=[CH:4][CH:3]=1.B1(B2OC(C)(C)C(C)(C)O2)OC(C)(C)C(C)(C)O1.[C:34]([O-:37])(=O)[CH3:35].[K+].C(Cl)Cl.[NH2:42][C:43]1[C:44]([C:50]2[O:54][C:53]([C:55]3[CH:60]=CC(CC([O-])=O)=[CH:57][CH:56]=3)=[N:52][N:51]=2)=[N:45][C:46](Br)=[CH:47][N:48]=1.C([O-])([O-])=O.[Na+].[Na+]>O1CCOCC1.CN(C=O)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[NH2:42][C:43]1[C:44]([C:50]2[O:54][C:53]([C:55]3[CH:60]=[CH:35][C:34]([OH:37])=[CH:57][CH:56]=3)=[N:52][N:51]=2)=[N:45][C:46]([C:2]2[CH:7]=[CH:6][C:5]([S:8]([CH2:11][CH2:12][N:13]([CH3:15])[CH3:14])(=[O:10])=[O:9])=[CH:4][CH:3]=2)=[CH:47][N:48]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 6

HCID 6344DichloromethaneHCID 10340Sodium CarbonateHCID 517044Potassium AcetateHCID 2733548Bis(pinacolato)diboraneHCID 68494241HCID 68494241, VerbindungHCID 86645024[4-[5-(3-Amino-6-bromo-pyrazin-2-yl)-1,3,4-oxadiazol-2-yl]phenyl]acetate

Produkt 1

HCID 136117292HCID 136117292, VerbindungAusbeute 15,3 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 178418476HCID 178418476, VerbindungKatalysatorHCID 6228DimethylformamideLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

2-(4-bromophenyl)sulfonyl-N,N-dimethyl-ethanamine (181.8 mg, 0.6221 mmol) was dissolved in dioxane (2 mL) and bis(pinacolato)diboron (237.0 mg, 0.9332 mmol) and potassium acetate (183.1 mg, 1.866 mmol) were added. The reaction mixture was degassed and filled with nitrogen (5×) then Pd(dppf)Cl2.CH2Cl2 (50.80 mg, 0.06221 mmol) was added and the reaction heated to 90° C. for 2 hours. The reaction mixture was cooled to ambient temperature and diluted with DMF (2 mL). [4-[5-(3-amino-6-bromo-pyrazin-2-yl)-1,3,4-oxadiazol-2-yl]phenyl]acetate (234 mg, 0.6221 mmol), Na2CO3 (933.0 μL of 2 M aqueous solution, 1.866 mmol) and Pd(PPh3)2Cl2 (43.67 mg, 0.06221 mmol) were added and the reaction heated at 150° C. under microwave conditions for 30 minutes. The reaction mixture was partitioned between EtOAc (5 mL) and water (5 mL) and any precipitate removed by filtration. The layers were separated and the aqueous layer extracted with EtOAc (3×5 mL) and the combined organic extracts dried over MgSO4, filtered and concentrated in vacuo. The residue was tritruated form EtOAc/MeOH to give the title compound as a brown solid (44.3 mg, 15%); 1H NMR (400 MHz, DMSO) d 2.07 (s, 6H), 2.56 (t, 2H), 3.52 (t, 2H), 7.03 (d, 2H), 7.87 (br s, 2H), 8.02 (dd, 4H), 8.38 (d, 2H), 9.05 (s, 1H) and 10.44 (s, 1H) ppm; MS (ES+) 467.2

Aufarbeitung

  1. customThe reaction mixture was degassed
  2. additionfilled with nitrogen (5×)
  3. temperatureThe reaction mixture was cooled to ambient temperature
  4. temperaturethe reaction heated at 150° C. under microwave conditions for 30 minutes
  5. customThe reaction mixture was partitioned between EtOAc (5 mL) and water (5 mL)
  6. customany precipitate removed by filtration
  7. customThe layers were separated
  8. extractionthe aqueous layer extracted with EtOAc (3×5 mL)
  9. dry with materialthe combined organic extracts dried over MgSO4
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-4545042879d04bc3b0ad9aa4492d9021
Quelldatensatz
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09365557B2

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