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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 592144Erstellt: 25. Oktober 2026

Diisopropylethylamine → 2-(4-(2-methylpyridin-4-yl)phenyl)-N-(6-morpholinopyridin-3-yl)acetamide

https://huagongshe.com/reaction/592144

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt6-(Morpholino)pyridin-3-amineHCID 104059—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt[4-(2-Methyl-pyridin-4-yl)-phenyl]-acetic acidHCID 58447644—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(4-(2-methylpyridin-4-yl)phenyl)-N-(6-morpholinopyridin-3-yl)acetamideHCID 58447751—

Reaktionsschritte

A mixture of 2-(4-(2-methylpyridin-4-yl)phenyl)acetic acid 73-1 (40 mg, 0.18 mmol), 6-morpholinopyridin-3-amine (40 mg, 0.22 mmol) and HATU (80 mg, 0.21 mmol) in 2 mL DMF was added DIEA (104 μL, 0.6 mmol) at room temperature. The mixture was stirred at room temperature for 2 hours. The solvent was removed by rotary evaporation. The crude product was purified by reverse phase HPLC to give the title compound 73 as white solid. MS m/z 389.19 (M+1); 1H NMR 400 MHz (DMSO-d6) δ11.30(s, 1H), 8.82(d, 1H, J=6.4 Hz), 8.57(d, 1H, J=2.4 Hz), 8.35(m, 1H), 8.24(dd, 1H, J1=6.4 Hz, J2=1.6 Hz), 8.19(dd, 1H, J1=10.0 Hz, J2=2.8 Hz), 8.02(m, 2H), 7.63(m, 2H), 7.42(d, 2H, J=9.6 Hz), 3.87(s, 2H), 3.75(m, 4H), 3.66(m, 4H), 2.80(s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09238646B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-2072c16d748d48e1a7a3453a29720239
Quellennotizuspto-grants-2016_01