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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1887852Erstellt: 25. Oktober 2026

4-Piperidinemethanol → 4-hydroxymethyl-3,4,5,6-tetrahydro-2H[1,2']bipyridinyl-5'-carboxylic acid (7-chloro-2-dimethylcarbamoyl-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-amide

https://huagongshe.com/reaction/1887852

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-PiperidinemethanolHCID 420771—
Edukt7-Chloro-3-{[(6-chloro-pyridine-3-carbonyl)-amino]-methyl}-4-oxo-1-phenyl-1,4-dihydro-quinoline-2-carboxylic acid dimethylamideHCID 71811128—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt4-hydroxymethyl-3,4,5,6-tetrahydro-2H[1,2']bipyridinyl-5'-carboxylic acid (7-chloro-2-dimethylcarbamoyl-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-amideHCID 71217337—

Reaktionsbedingungen

Temperatur125 °C

Reaktionsschritte

The intermediate 7-chloro-3-{[(6-chloro-pyridine-3-carbonyl)-amino]-methyl}-4-oxo-1-phenyl-1,4-dihydro-quinoline-2-carboxylic acid dimethylamide (70 mg, 0.141 mmol) was combined with piperidin-4-ylmethanol (40 mg, 0.346 mmol) and NMP (2 mL). The reaction mixture was heated at 125° C. for 2 hr. After this time, the crude product was subjected to preparative reverse-phase HPLC purification. The product, 4-hydroxymethyl-3,4,5,6-tetrahydro-2H[1,2′]bipyridinyl-5′-carboxylic acid (7-chloro-2-dimethylcarbamoyl-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-amide was obtained as 30 mg (37%) of a white solid. MS calcd. for C31H32ClN5O4 [(M+H)+] 574.2, obsd. 574.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08501732B2
Quelldatensatzuspto-grants-2013_08
ORD IDord-fcd5459c231d4cd9b7cb16ab2d3e4a8a
Quellennotizuspto-grants-2013_08