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HRID 69152作成日:2026年10月24日

N-Methoxy-N-methylquinoline-6-carboxamide → 1-(Quinolin-6-yl)ethan-1-one

https://huagongshe.com/ja/reaction/69152

反応式

関与物質

役割名称HCID仕込み量
反応物N-Methoxy-N-methylquinoline-6-carboxamideHCID 55211172—
反応物HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
溶媒Tetrahydrofuran tolueneHCID 22635083—
生成物1-(Quinolin-6-yl)ethan-1-oneHCID 258559—

反応条件

温度0 °C

反応手順

Methylmagnesium bromide (190 mL of a 1.4 M solution in toluene/THF 3:1, 270 mmol) was added over 35 min to a solution of quinoline-6-carboxylic acid methoxy-methyl-amide (Stage 1.5, 26 g, 120 mmol) in THF at 0° C. under nitrogen. The RM was stirred for 30 min at 0° C. and then allowed to warm up to rt. The RM was quenched with 1 M HCl and the THF removed under reduced pressure. The residue was taken up in EtOAc and the organic layer separated, dried and concentrated to give the title compound as a yellow solid (tR 1.0 min (conditions 1), MH+=172).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822468B2
出典データセットuspto-grants-2014_09
ORD IDord-b400a060e54b478684a09a7f1a29c10e
出典メモuspto-grants-2014_09