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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1472573Erstellt: 24. Oktober 2026

Potassium Phosphate, Tribasic → 2-(2-Chloro-5-cyanopyridin-4-ylamino)-N-methylbenzamide

https://huagongshe.com/de/reaction/1472573

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
EduktBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
Edukt2-Amino-N-methoxybenzamideHCID 12392707—
Edukt6-Chloro-4-iodopyridine-3-carbonitrileHCID 57516912—
KatalysatorPalladium (II) acetateHCID 4144353—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-(2-Chloro-5-cyanopyridin-4-ylamino)-N-methylbenzamideHCID 57516913740,3%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 6-chloro-4-iodo-nicotinonitrile (14 g, 53.03 mmole, 1 eq), 2-amino-N-methoxy-benzamide (7.96 g, 53.03 mmole, 1 eq) and K3PO4 (28.14 g, 132.57 mmole, 2.5 eq) in 1,4-dioxane (250 mL) was degassed with N2 for 1 h. To this mixture were added Pd(OAC)2 (0.238 g, 1.06 mmole, 0.02 eq) and DPEPhos (2.28 g, 4.24 mmole, 0.08 eq). The resulting reaction mixture was degassed with N2 for another 15 min after which the resulting reaction mixture was stirred at 110° C. overnight. After completion of reaction solid material was collected by filtration, dissolved in water (500 mL), and extracted with ethyl acetate (5×200 mL). Combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure to give crude material. It was purified by column chromatography over silica gel (60-120 mesh) using 0.2% methanolic ammonia (10% ammonia in MeOH) in dichloromethane as the eluant to give the title compound as a pale yellow solid (9 g, 59%). 1H-NMR (400 MHz, DMSO-d6): δ 2.75 (d, 3H, J=4.56 Hz), 7.09 (s, 1H), 7.25-7.35 (m, 1H), 7.53-7.60 (m, 2H), 7.72 (d, 1H, J=7.48 Hz), 8.56 (s, 1H), 8.69-8.79 (brs, 1H), 10.65 (s, 1H). LC-MS calculated for C14H11ClN4O (M+H) 287.06. found 286.9.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09012479B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-96c5f4f1208a49b7817fe80ec6b61e7a
Quellennotizuspto-grants-2015_04