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Cesium carbonate → Ethyl 4-(2,4-diamino-3-methoxycarbonylphenyl)-furan-3-carboxylate

HRID 1778403
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1778403
[NH2:1][C:2]1[C:11](Br)=[CH:10][CH:9]=[C:8]([NH2:13])[C:3]=1[C:4]([O:6][CH3:7])=[O:5].COC([C:18]1[O:19][CH:20]=[CH:21][C:22]=1B(O)O)=O.F[B-](F)(F)F.C([PH+]([C:40]([CH3:43])(C)C)C(C)(C)C)(C)(C)C.[C:44](=O)([O-:46])[O-:45].[Cs+].[Cs+]>O1CCOCC1.O.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[NH2:1][C:2]1[C:3]([C:4]([O:6][CH3:7])=[O:5])=[C:8]([NH2:13])[CH:9]=[CH:10][C:11]=1[C:21]1[C:22]([C:44]([O:46][CH2:40][CH3:43])=[O:45])=[CH:18][O:19][CH:20]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 10796Cesium carbonateHCID 2734635Tri-tert-butylphosphine tetrafluoroborateHCID 66685498[2-(Methoxycarbonyl)furan-3-yl]boronic acidHCID 66685632Methyl 2,6-diamino-3-bromobenzoate2×

Produkt 1

HCID 66685491Ethyl 4-(2,4-diamino-3-methoxycarbonylphenyl)-furan-3-carboxylateAusbeute 689,8 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 9811564Bis(dibenzylideneacetone)palladiumKatalysatorHCID 962WaterLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

A mixture of methyl 2,6-diamino-3-bromobenzoate (Intermediate 90, 1.0 g), 2-methoxycarbonyl-furan-3-boronic acid (0.980 g), tris-(dibenzylideneacetone)-dipalladium (0.188 g), tri-tert-butylphosphonium tetrafluoroborate (0.119 g) and cesium carbonate (4.0 g) in dioxane (45 mL) and water (6 mL) was de-gassed and flushed with argon. The resultant mixture was stirred at room temperature for 1 hour, then heated at 70° C. for 1 hour. The mixture was cooled, diluted with ethyl acetate and washed with water, dried (MgSO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and pentane, with a gradient of 20-50% to give ethyl 4-(2,4-diamino-3-methoxycarbonylphenyl)-furan-3-carboxylate (0.861 g).

Aufarbeitung

  1. customwas de-gassed
  2. customflushed with argon
  3. temperatureheated at 70° C. for 1 hour
  4. temperatureThe mixture was cooled
  5. additiondiluted with ethyl acetate
  6. washwashed with water
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationThe filtrate was concentrated in vacuo
  10. customthe residue was purified by chromatography on silica
  11. washeluting with a mixture of ethyl acetate and pentane, with a gradient of 20-50%

Quellen und Nachweise

ORD-Eintrag
ord-52135b162fed41f4b890d3e57a9629fe
Quelldatensatz
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09266896B2

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