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HRID 1170325作成日:2026年10月27日

N-Dimethylaminomethylene-isonicotinamide → 2-[4-(5-Pyridin-4-yl-[1,2,4]triazol-1-yl)-phenoxymethyl]-quinoline

https://huagongshe.com/reaction/1170325

反応式

関与物質

役割名称HCID仕込み量
反応物N-Dimethylaminomethylene-isonicotinamideHCID 12569643—
反応物4-(Quinolin-2-ylmethoxy)phenylhydrazineHCID 15225068—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物2-[4-(5-Pyridin-4-yl-[1,2,4]triazol-1-yl)-phenoxymethyl]-quinolineHCID 1166088021.8%

反応手順

Isonicatinamide (4.15 g) was heated in 35 ml of N,N-Dimethylformamide diethyl acetal at reflux for 3 h. The reaction mixture was cooled to ambient temperature and concentrated to give 5.02 g of N-Dimethylaminomethylene-isonicotinamide. To a solution of [4-(Quinolin-2-ylmethoxy)-phenyl]-hydrazine (3.16 g) in methanol (30 mL) and acetic acid (2.5 mL) was added N-Dimethylaminomethylene-isonicotinamide (1.10 g) and the reaction mixture heated at reflux for 72 h. The reaction mixture was concentrated onto silica gel and purified by flash chromatography to provided the title compound (514 mg). 1H NMR (400 MHz, CDCl3) δ 8.60 (d, J=5.8 Hz, 2H), 8.22 (d, J=8.7 Hz, 1H), 8.10 (s, 1H), 8.07 (d, J=8.7 Hz, 1H), 7.85 (d, J=7.1 Hz, 1H), 7.76 (m, 1H), 7.66 (d, J=8.3 Hz, 1H), 7.56 (m, 1H), 7.56 (m, 1H), 7.38 (d, J=6.2 Hz, 2H), 7.26 (d, J=8.7 Hz, 2H), 7.11 (d, J=9.1 Hz, 2H), 5.42 (s, 2H); MS: (M+H m/z=380.3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07825254B2
出典データセットuspto-grants-2010_11
ORD IDord-af0e945ee77e49dbace5e31d4c8d9097
出典メモuspto-grants-2010_11