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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1174753Erstellt: 25. Oktober 2026

3-Amino-6-chloro-2-picoline → 4-[6-(6-Chloro-2-methyl-pyridin-3-ylamino)-5-methyl-pyrimidin-4-yloxy]-piperidine-1-carboxylic Acid Isopropyl Ester

https://huagongshe.com/reaction/1174753

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Amino-6-chloro-2-picolineHCID 7009500—
Edukt4-(6-Chloro-5-methyl-pyrimidin-4-yloxy)-piperidine-1-carboxylic acid isopropyl esterHCID 11493357—
EduktSodium t-butoxideHCID 23676156—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorBiphenyl-3-yl-di-tert-butyl-phosphaneHCID 67201513—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-[6-(6-Chloro-2-methyl-pyridin-3-ylamino)-5-methyl-pyrimidin-4-yloxy]-piperidine-1-carboxylic Acid Isopropyl EsterHCID 1124713931%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of 4-(6-chloro-5-methyl-pyrimidin-4-yloxy)-piperidine-1-carboxylic acid isopropyl ester (1.546 g, 4.93 mmol), palladium acetate (110 mg, 0.49 mmol), biphenyl-3-yl-di-tert-butyl-phosphane (18.5 mg, 0.062 mmol), sodium tert-butoxide (1.20 g, 12.5 mmol), and 6-chloro-2-methyl-pyridin-3-ylamine (709 mg, 4.97 mmol) in 15 mL dioxane was heated in microwave for 2 hour at 120° C. Solids were filtered off and mixture was purified to give Compound A90 as a tanned solid (640 mg, 31%). 1H NMR (CDCl3, 400 MHz) δ 1.11-1.12 (d, 6H), 1.52-1.62 (m, 2H), 1.81-1.89 (m, 2H), 1.98 (s, 3H), 2.23 (m, 3H), 3.21-3.30 (m, 2H), 3.59-3.70 (m, 3H), 5.14-5.17 (m, 1H), 6.83-6.91 (m, 1H), 7.14-7.16 (d, 1H), 7.55-7.57 (d, 1H), 7.87 (s, 1H). Exact mass calculated for C20H26ClN5O3 419.17, found 419.9 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07838525B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-4b343de078ce42c8a82909b331fffaa2
Quellennotizuspto-grants-2010_11