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Potassium Carbonate → Hydrochloric Acid

HRID 912014
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 912014
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([N:14]2[CH:18]=[C:17](B3OC(C)(C)C(C)(C)O3)[CH:16]=[N:15]2)[CH2:10][CH2:9]1)=O)(C)(C)C.Br[C:29]1[C:33]2[CH:34]=[N:35][C:36]([NH2:50])=[C:37]([O:38][CH:39]([C:41]3[C:46]([Cl:47])=[CH:45][CH:44]=[C:43]([F:48])[C:42]=3[Cl:49])[CH3:40])[C:32]=2[O:31][CH:30]=1.C(=O)([O-])[O-].[K+].[K+]>COCCOC.O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Cl:49][C:42]1[C:43]([F:48])=[CH:44][CH:45]=[C:46]([Cl:47])[C:41]=1[CH:39]([O:38][C:37]1[C:32]2[O:31][CH:30]=[C:29]([C:17]3[CH:16]=[N:15][N:14]([CH:11]4[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]4)[CH:18]=3)[C:33]=2[CH:34]=[N:35][C:36]=1[NH2:50])[CH3:40].[ClH:47]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 3

HCID 11430Potassium CarbonateHCID 45480279tert-butyl 4-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylateHCID 674022843-Bromo-7-[1-(2,6-dichloro-3-fluorophenyl)ethoxy]furo[3,2-c]pyridin-6-ylamine

Produkt 2

HCID 313Hydrochloric AcidHCID 57812483
7-[1-(2,6-Dichloro-3-fluorophenyl)ethoxy]-3-(1-piperidin-4-yl-1H-pyrazol-4-yl)-furo[3,2-c]pyridin-6-ylamine

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 178418397HCID 178418397, VerbindungKatalysatorHCID 962WaterLösungsmittelHCID 80711,2-DimethoxyethaneLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To a stirred mixture of 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrazol-1-yl]-piperidine-1-carboxylic acid tert-butyl ester (26.94 mg, 0.071 mmol), 3-bromo-7-[1-(2,6-dichloro-3-fluorophenyl)ethoxy]furo[3,2-c]pyridin-6-ylamine (20.0 mg, 0.047 mmol), potassium carbonate (19.7 mg, 0.14 mmol) in DME (2.0 mL) and H2O (0.40 mL) was added Pd(PPh3)4 (2.8 mg, 0.0024 mmol) under Nitrogen. The resulting mixture was refluxed at 100° C. for 30 min. LC-MS indicated completion of reaction. The solvent was then removed under reduced pressure and the resulting residue was purified by a flash chromatography (2% MeOH in DCM). MS (ES+): m/z 590.07, 592.08 (MH+). HPLC: tR=3.48 min (ZQ3, polar—5 min). The product purified above was then dissolved in 2 mL dioxane, to this solution was added solution of 4 N HCl in dioxane (1 mL) at r.t., the resulting mixture was stirred at r.t. for 1.5 h. LC-MS indicated completion of reaction. The solvent was removed under reduced pressure to give the title compound as HCl salt. The 1H NMR spectrum matches that of Example 5.

Aufarbeitung

  1. customcompletion of reaction
  2. customThe solvent was then removed under reduced pressure
  3. customthe resulting residue was purified by a flash chromatography (2% MeOH in DCM)
  4. custom5 min
  5. customThe product purified above
  6. dissolutionwas then dissolved in 2 mL dioxane, to this solution
  7. additionwas added solution of 4 N HCl in dioxane (1 mL) at r.t.
  8. customcompletion of reaction
  9. customThe solvent was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-e37e9154ed2f4b948cfd02b8cc6ea934
Quelldatensatz
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08022206B2

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