1-Methoxy-2-propanol → HCID 66711135, Verbindung

HRID 1261993Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1261993
CS([C:4]1[N:9]=[CH:8][C:7]2=[CH:10][CH:11]=[C:12]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[O:19][CH3:20])[N:6]2[N:5]=1)=O.C(N(CC)C(C)C)(C)C.[N:30]1([CH:36]2[CH2:41][CH2:40][N:39]([C:42]3[CH:47]=[CH:46][C:45]([NH2:48])=[CH:44][CH:43]=3)[CH2:38][CH2:37]2)[CH2:35][CH2:34][O:33][CH2:32][CH2:31]1.COCC(O)C>>[CH3:20][O:19][C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=1[C:12]1[N:6]2[C:7]([CH:8]=[N:9][C:4]([NH:48][C:45]3[CH:46]=[CH:47][C:42]([N:39]4[CH2:38][CH2:37][CH:36]([N:30]5[CH2:35][CH2:34][O:33][CH2:32][CH2:31]5)[CH2:41][CH2:40]4)=[CH:43][CH:44]=3)=[N:5]2)=[CH:10][CH:11]=1

Komponenten

5

Edukt 4

HCID 79001-Methoxy-2-propanolHCID 81531DiisopropylethylamineHCID 210915834-(4-Morpholinopiperidin-1-yl)anilineHCID 667107912-Methanesulfinyl-7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazine

Produkt 1

HCID 66711135HCID 66711135, VerbindungAusbeute 21 %

Versuchsvorschrift

2-Methanesulfinyl-7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazine (125.0 mg, 0.0004350 mol), N,N-Diisopropylethylamine (0.114 mL, 0.000652 mol) and 4-(4-Morpholin-4-yl-piperidin-1-yl)-phenylamine (0.227 g, 0.000870 mol) were dissolved in 1-Methoxy-2-propanol (1.2 mL, 0.013 mol) and The reaction was irradiated at 300 watts, 180° C. for 40 minutes or until HPLC showed consumption of starting material. The reaction mixture was then reduced en vacuo and the product was isolated and purified by Gilson prep HPLC to afford 44.36 mg of [7-(2-Methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-[4-(4-morpholin-4-yl-piperidin-1-yl)-phenyl]-amine as a lyophilized powder. (M+H)=485.8. 1H NMR (400 MHz, DMSO, d6) δ 9.20 (s, 1H), 8.91 (s, 1H), 7.82 (dd, 1H, J=1.56, 6.16 Hz), 7.60 (d, 2H, J=9.01 Hz), 7.45 (m, 1H), 7.21 (d, 1H, J=8.17 Hz), 7.12 (t, 1H, J=7.28 Hz), 6.90 (m, 4H), 4.02 (m, 2H), 3.80 (s, 3H), 3.50 (m, 5H), 3.35 (m, 2H), 3.24 (m, 2H), 2.71 (m, 2H), 2.12 (m, 2H), 1.70 (m, 2H).

Aufarbeitung

  1. customThe reaction was irradiated at 300 watts, 180° C. for 40 minutes or until HPLC
  2. customconsumption of starting material
  3. customthe product was isolated
  4. custompurified by Gilson prep HPLC

Quellen und Nachweise

ORD-Eintrag
ord-7e65ba4fb715482f9f1bfdb4b5dcd283
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08471005B2

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