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Sodium Carbonate → N-{4-[2-(4-fluorophenyl)-7-methyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazin-3-yl]pyridin-2-yl}propanamide

HRID 570136
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 570136
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:17](B3OC(C)(C)C(C)(C)O3)=[C:11]3[O:12][CH2:13][CH2:14][CH:15]([CH3:16])[N:10]3[N:9]=2)=[CH:4][CH:3]=1.Br[C:28]1[CH:33]=[CH:32][N:31]=[C:30]([NH:34][C:35](=[O:38])[CH2:36][CH3:37])[CH:29]=1.C([O-])([O-])=O.[Na+].[Na+]>O1CCOCC1.C1CCC(P(C2CCCCC2)C2CCCCC2)CC1.C1CCC(P(C2CCCCC2)C2CCCCC2)CC1.[Cl-].[Cl-].[Pd+2]>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:17]([C:28]3[CH:33]=[CH:32][N:31]=[C:30]([NH:34][C:35](=[O:38])[CH2:36][CH3:37])[CH:29]=3)=[C:11]3[O:12][CH2:13][CH2:14][CH:15]([CH3:16])[N:10]3[N:9]=2)=[CH:6][CH:7]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 10340Sodium CarbonateHCID 67073822N-(4-bromopyridin-2-yl)propanamideHCID 894883172-(4-fluorophenyl)-7-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine

Produkt 1

HCID 89488349N-{4-[2-(4-fluorophenyl)-7-methyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazin-3-yl]pyridin-2-yl}propanamideAusbeute 23,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 11556747Bis(tricyclohexylphosphine)palladium(II) DichlorideKatalysator
HCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

150 mg of 2-(4-fluorophenyl)-7-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine (0.419 mmol, 1.1 eq.) and 87 mg of N-(4-bromopyridin-2-yl)propanamide (0.381 mmol, 1 eq.) are dissolved in 1.5 ml of 1,4-dioxane. To this solution are added 22 mg of bis(tricyclohexylphosphine)-palladium(II)dichloride (0.03 mmol, 0.08 eq) and a aqueous solution of Na2CO3 (5 eq, 0.952 ml). The reaction mixture is flushed for 5 mins with argon and then sealed. Next the mixture is heated for 15 mins at 120° C. in the microwave (CEM Explorer). After cooling, the reaction mixture is diluted with EtOAc and washed with water. The combined organic phase are dried over Na2SO4 and concentrated in vacuo. The crude product is purified by silica gel chromatography (eluent cyclohexane/ethyl acetate). 34 mg (21%) of N-{4-[2-(4-fluorophenyl)-7-methyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazin-3-yl]pyridin-2-yl}propanamide are obtained.

Aufarbeitung

  1. customThe reaction mixture is flushed for 5 mins with argon
  2. customsealed
  3. temperatureAfter cooling
  4. additionthe reaction mixture is diluted with EtOAc
  5. washwashed with water
  6. dry with materialThe combined organic phase are dried over Na2SO4
  7. concentrationconcentrated in vacuo
  8. customThe crude product is purified by silica gel chromatography (eluent cyclohexane/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-fb6540000e2b499aa0536deabc6de2b9
Quelldatensatz
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09023844B2

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