4-Butyloxyaniline → N2-(4-n-Butyloxyphenyl)-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-2,4-pyridinediamine

HRID 226836

Reaktionsgleichung

Reaktionsgleichung von HRID 226836
Cl[C:2]1[N:7]=[C:6]([NH:8][C:9]2[CH:14]=[CH:13][C:12]3[O:15][CH2:16][CH2:17][O:18][C:11]=3[CH:10]=2)[C:5]([F:19])=[CH:4][N:3]=1.[CH:20](N(CC)C(C)C)(C)C.[CH2:29]([O:33][C:34]1[CH:40]=[CH:39][C:37](N)=[CH:36][CH:35]=1)[CH2:30][CH2:31][CH3:32]>C(O)CO>[CH2:29]([O:33][C:34]1[CH:40]=[CH:39][C:37]([NH:7][C:2]2[CH:20]=[C:6]([NH:8][C:9]3[CH:14]=[CH:13][C:12]4[O:15][CH2:16][CH2:17][O:18][C:11]=4[CH:10]=3)[C:5]([F:19])=[CH:4][N:3]=2)=[CH:36][CH:35]=1)[CH2:30][CH2:31][CH3:32]

Komponenten

5

Edukt 3

HCID 203524-ButyloxyanilineHCID 81531DiisopropylethylamineHCID 220603622-chloro-5-fluoro-N-(3,4-ethylenedioxyphenyl)-4-pyrimidineamine

Produkt 1

HCID 22060376N2-(4-n-Butyloxyphenyl)-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-2,4-pyridinediamineAusbeute 49,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 174Ethylene GlycolLösungsmittel

Reaktionsbedingungen

Temperatur
185 °C

Versuchsvorschrift

To a magnetically stirred solution of 2-chloro-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-4-pyrimidineamine (0.25 g, 0.89 mmol) in ethylene glycol (3.0 mL) under nitrogen at room temperature was added N,N-diisopropylethylamine (0.12 g, 0.89 mmol) followed by 4-butoxyaniline (0.18 g, 1.1 mmol). The reaction mixture was heated to 185° C. for 5 h, cooled to room temperature, and partitioned between water (20 mL) and ethyl acetate (20 mL). The aqueous layer was extracted with ethyl acetate (20 mL) and the combined organic layers were dried (Na2SO4), filtered and concentrated in vacuo. The crude brown solid was purified by chromatography (silica gel, 2:1 hexanes/ethyl acetate) to afford N2-(4-n-Butyloxyphenyl)-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-2,4-pyridinediamine (0.18 g, 49%) as a tan solid: Rf0.66 (silica gel, 4:1 chloroform/ethyl acetate); mp 133–135° C.; 1H NMR (300 MHz, CDCl3) δ 7.89 (d, J=3.2 Hz, 1H), 7.39 (d, J=8.9 Hz, 2H), 7.28 (d, J=2.5 Hz, 1H), 6.95 (dd, J=8.7, 2.5 Hz, 1H) 6.90–6.81 (m, 4H), 6.60 (d, J=2.4 Hz, 1H), 4.27 (s, 4H), 3.94 (t, J=6.5 Hz, 2H), 1.80–1.71 (m, 2H), 1.55–1.42 (m, 2H), 0.97 (t, J=7.3 Hz, 3H); 13C NMR (75 MHz, CDCl3) δ 156.3, 155.1, 150.4, 143.6, 142.7, 140.3, 140.0, 139.4, 133.0, 131.7, 121.9, 117.3, 115.0, 114.7, 110.8, 68.2, 64.7, 64.5, 31.6, 19.4, 14.0; IR (ATR) 3356 cm1; ESI MS m/z 411 [C22H23FN4O3+H]+; HPLC (Method A)>99% (AUC), tR=17.3 mm. Anal. Calcd for C22H23FN4O3: C, 64.38; H, 5.65; N, 13.65. Found C, 62.64; H, 5.59; N, 13.15.

Aufarbeitung

  1. temperaturecooled to room temperature
  2. custompartitioned between water (20 mL) and ethyl acetate (20 mL)
  3. extractionThe aqueous layer was extracted with ethyl acetate (20 mL)
  4. dry with materialthe combined organic layers were dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe crude brown solid was purified by chromatography (silica gel, 2:1 hexanes/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-bf5668fea8484daaacdc74b2a5bf2d26
Quelldatensatz
uspto-grants-2009_07
Patentnummer
US07557210B2

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