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HRID 1925140作成日:2026年10月24日

Methyl 3-Bromopyruvate → HCID 59233216、化合物

https://huagongshe.com/ja/reaction/1925140

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-BromopyruvateHCID 352524—
反応物Sodium BicarbonateHCID 516892—
反応物HCID 59233207HCID 59233207—
溶媒1,4-DioxaneHCID 31275—
生成物HCID 59233216HCID 59233216—

反応条件

温度80 °C

反応手順

A reaction mixture of 6-((6-bromo-[1,2,4]triazolo[4,3-a]pyridin-3-yl)difluoromethyl)pyridazin-3-amine (11.0 g, 32.2 mmol), methyl 3-bromo-2-oxopropanoate (11.67 g, 64.5 mmol), and NaHCO3 (10.84 g) in dioxane (150 mL) was heated at 80° C. for 4 hrs to provide a red reaction mixture. Solids were filtered off, rinsed with dioxane, and the combined filtrates were concentrated via rotary evaporation. The resulting residue was dissolved in EtOAc and washed with 0.1 N NaOH until the red color no longer persisted. The organic phase was then separated and concentrated to dryness. The resulting material was purified via MPLC (5:95, MeOH/EtOAc) to provide the title compound, 45I (4.0 g, 9.45 mmol, 30%). 1H NMR (400 MHz, DMSO-d6) δ ppm 3.88 (s, 3 H) 7.77 (dd, J=9.73, 1.64 Hz, 1 H) 7.85 (d, J=9.60 Hz, 1 H) 7.97-8.08 (m, 1 H) 8.53 (d, J=9.60 Hz, 1 H) 8.98 (d, J=1.01 Hz, 1 H) 9.02 (s, 1 H). ESI-MS:m/z 423.1 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08178534B2
出典データセットuspto-grants-2012_05
ORD IDord-8969949d90cd41ceb02c5d5572e19037
出典メモuspto-grants-2012_05