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2,4-Dichloropyridine → N-(4-chloro-2-pyridinyl)-1,3-oxazol-2-amine

HRID 359
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 359
Clc1ccnc(Cl)c1.Nc1ncco1>C1COCCO1.CC1(C)c2cccc(P(c3ccccc3)c3ccccc3)c2Oc2c(P(c3ccccc3)c3ccccc3)cccc21.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C([O-])[O-].[Cs+].[Cs+].[Pd].[Pd]>Clc1ccnc(Nc2ncco2)c1
KomponentenReaktionsbedingungenVersuchsvorschriftQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 2

HCID 335152,4-DichloropyridineHCID 5585212-Aminooxazole

Produkt 1

HCID 130016260N-(4-chloro-2-pyridinyl)-1,3-oxazol-2-amineAusbeute 2,02 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 10796Cesium carbonateReagenzHCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)
Katalysator
HCID 9811564Bis(dibenzylideneacetone)palladiumKatalysator
HCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

Objective: To isolate some of the required product to provide an analytical sample for a large catalyst screen. 2,4-dichloropyridine (0.109 mL, 1.01 mmol), oxazol-2-amine (85 mg, 1.01 mmol), TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (22.89 mg, 0.02 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (44.0 mg, 0.08 mmol) (Xantphos) and cesium carbonate (660 mg, 2.03 mmol) were added to a microwave vail and the vial was purged with nitrogen. Degassed dioxane (4 mL) was then added and the reaction mixture was heated to 140 °C for 1 h under microwave irradiation. LCMS of crude reaction mixture showed some of the required product was formed, however the LCMS using acidic modifier was somewhat misleading as a side- product co-elutes with the required product thus giving the impression that a greater amount of product was formed than is the case. LCMS under acidic modifier is more informative. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% heptane in EtOAc. Pure fractions were evaporated to dryness to afford N-(4-chloropyridin-2-yl)oxazol-2-amine (4.00 mg, 2.018 %) as a pale yellow residue. Conclusion: 4 mg of impure product was isolated.

Quellen und Nachweise

ORD-Eintrag
ord-bc6c718e90df4b2591cc2506c375ce3f
Quelldatensatz
750 AstraZeneca ELN dataset
Originallink
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