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HRID 1978960Erstellt: 24. Oktober 2026

2,4,6-Trimethylpyridine → N-[(4-chlorophenyl)methyl]-7-methyl-4-oxo-2-(thiomorpholinomethyl)thieno[2,3-b]pyridine-5-carboxamide

https://huagongshe.com/reaction/1978960

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,6-TrimethylpyridineHCID 7953—
EduktMethanesulfonyl chlorideHCID 31297—
EduktThiomorpholineHCID 67164—
EduktN-[(4-chlorophenyl)methyl]-2-(hydroxymethyl)-7-methyl-4-oxo-thieno[2,3-b]pyridine-5-carboxamideHCID 6482399—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[(4-chlorophenyl)methyl]-7-methyl-4-oxo-2-(thiomorpholinomethyl)thieno[2,3-b]pyridine-5-carboxamideHCID 648240560%

Reaktionsschritte

To a solution of N-(4-chlorobenzyl)-2-(hydroxymethyl)-7-methyl-4-oxo-4,7-dihydrothieno[2,3-b]pyridine-5-carboxamide (0.300 g) from Example No. 35 in DMF (16 mL) are added DMAP (16 mg), 2,4,6-collidine (0.27 mL), and methanesulfonyl chloride (0.16 mL). The reaction mixture is stirred at room temperature for 2 h and then thiomorpholine (0.83 mL) is added. The mixture is stirred at room temperature for 3 d and is then poured into water (50 mL). The resulting off-white solid is filtered off and recrystallized from ethanol to yield 0.222 g (60%) of the title compound as an off-white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06239142B1
Quelldatensatzuspto-grants-2001_05
ORD IDord-4ca572de4d224123b840374e88ef34e1
Quellennotizuspto-grants-2001_05