Tetrahydrofuran → N-(6-methoxypyridin-3-yl)-5-(4-methyl-6-(methylthio)-1,3,5-triazin-2-yl)pyrimidin-4-amine

HRID 1811926Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1811926
Br[C:2]1[C:3]([NH:8][C:9]2[CH:10]=[N:11][C:12]([O:15][CH3:16])=[CH:13][CH:14]=2)=[N:4][CH:5]=[N:6][CH:7]=1.[CH3:17][C:18]1[N:23]=[C:22]([S:24][CH3:25])[N:21]=[C:20]([Sn](CCCC)(CCCC)CCCC)[N:19]=1.[F-].[Cs+].C1COCC1>O.[Cu]I.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>[CH3:16][O:15][C:12]1[N:11]=[CH:10][C:9]([NH:8][C:3]2[C:2]([C:20]3[N:19]=[C:18]([CH3:17])[N:23]=[C:22]([S:24][CH3:25])[N:21]=3)=[CH:7][N:6]=[CH:5][N:4]=2)=[CH:14][CH:13]=1

Komponenten

8

Edukt 4

HCID 8028TetrahydrofuranHCID 25953Cesium fluorideHCID 601547172-Methyl-4-(methylthio)-6-(tributylstannyl)-1,3,5-triazineHCID 601557905-bromo-N-(6-methoxypyridin-3-yl)pyrimidin-4-amine

Produkt 1

HCID 60155791N-(6-methoxypyridin-3-yl)-5-(4-methyl-6-(methylthio)-1,3,5-triazin-2-yl)pyrimidin-4-amineAusbeute 53,7 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)KatalysatorHCID 178418397HCID 178418397, VerbindungKatalysatorHCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

A glass microwave reaction vessel was charged with 5-bromo-N-(6-methoxypyridin-3-yl)pyrimidin-4-amine (23 mg, 0.082 mmol), 2-methyl-4-(methylthio)-6-(tributylstannyl)-1,3,5-triazine (35.2 mg, 0.082 mmol), copper(I) iodide (15 mg, 0.082 mmol), cesium fluoride (206 mg, 0.82 mmol) and tetrakis(triphenylphosphine)palladium(0) (9.45 mg, 8.18 μmol) and THF (1 mL). The reaction mixture was stirred and heated in a Emrys Optimizer microwave reactor (Personal Chemistry, Biotage AB, Inc., Upssala, Sweden) at 140° C. for 30 min. The reaction mixture was diluted with water (10 mL) and extracted with EtOAc (2×30 mL). The organic extract was washed with saturated NaCl (5 mL) and dried over Na2SO4. The solution was filtered and concentrated in vacuo to give the crude product as a light-yellow solid. The crude product was purified by silica gel chromatography eluting with 60% EtOAc/hexanes to give N-(6-methoxypyridin-3-yl)-5-(4-methyl-6-(methylthio)-1,3,5-triazin-2-yl)pyrimidin-4-amine (15 mg, 0.044 mmol, 53.7% yield). 1H NMR (300 MHz, CDCl3) δ 11.58 (s, 1H); 9.65 (s, 1H); 8.74 (s, 1H); 8.35 (d, J=2.19 Hz, 1H); 8.07 (dd, J=8.84, 2.56 Hz, 1H); 6.82 (d, J=8.92 Hz, 1H); 3.96 (s, 3H); 2.67 (s, 3H); 2.65 (s, 3H). m/z (ESI, +ve ion) 342.0 (M+H)+.

Aufarbeitung

  1. customA glass microwave reaction vessel
  2. extractionextracted with EtOAc (2×30 mL)
  3. extractionThe organic extract
  4. washwas washed with saturated NaCl (5 mL)
  5. dry with materialdried over Na2SO4
  6. filtrationThe solution was filtered
  7. concentrationconcentrated in vacuo
  8. customto give the crude product as a light-yellow solid
  9. customThe crude product was purified by silica gel chromatography
  10. washeluting with 60% EtOAc/hexanes

Quellen und Nachweise

ORD-Eintrag
ord-8335519536014ff0b1dfb074d10c8752
Quelldatensatz
uspto-grants-2013_01
Patentnummer
US08362241B2

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