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HRID 340064作成日:2026年10月25日

Acetic Acid → 4,4-Diethoxy-3-{[6-[2-ethyl-5-fluoro-4-(2-trimethylsilanyl-ethoxymethoxy)-phenyl]-1-(tetrahydro-pyran-2-yl)-1H-indazole-3-carboximidoyl]-amino}-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/340064

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物tert-Butyl 3-amino-4,4-diethoxypiperidine-1-carboxylateHCID 53249937—
反応物6-[2-Ethyl-5-fluoro-4-(2-trimethylsilanyl-ethoxymethoxy)-phenyl]-1-(tetrahydro-pyran-2-yl)-1H-indazole-3-carboximidic acid methyl esterHCID 86676271—
溶媒EthanolHCID 702—
生成物4,4-Diethoxy-3-{[6-[2-ethyl-5-fluoro-4-(2-trimethylsilanyl-ethoxymethoxy)-phenyl]-1-(tetrahydro-pyran-2-yl)-1H-indazole-3-carboximidoyl]-amino}-piperidine-1-carboxylic acid tert-butyl esterHCID 178467534117.3%

反応条件

温度50 °C

反応手順

To a solution of 6-[2-ethyl-5-fluoro-4-(2-trimethylsilanyl-ethoxymethoxy)-phenyl]-1-(tetrahydro-pyran-2-yl)-1H-indazole-3-carboximidic acid methyl ester (Preparation 7, 31.4 g, 59.5 mmol) in ethanol (140 mL) was added a solution of 3-amino-4,4-diethoxy-piperidine-1-carboxylic acid tert-butyl ester (US-2004/0229862, 18.02 g, 62.48 mmol) in ethanol (100 mL). Acetic acid (6.81 mL, 119 mmol) was added and the reaction mixture was heated at 50° C. for 18 hours. The reaction mixture was concentrated in vacuo and azeotroped with toluene (100 mL) to give the title compound as a foam (54.7 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895544B2
出典データセットuspto-grants-2014_11
ORD IDord-e6d323f73bc84247a9c092c522d10273
出典メモuspto-grants-2014_11