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HRID 1252作成日:2026年10月24日

Ammonium formate → Amlodipine

https://huagongshe.com/ja/reaction/1252

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium formateHCID 2723923—
反応物4-(2-Chlorophenyl)-2-(2-hydroxyimino-ethoxymethyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylic acid 3-ethyl 5-methyl esterHCID 73078080—
触媒Palladium hydroxideHCID 9942167—
溶媒MethanolHCID 887—
生成物AmlodipineHCID 216260.7%

反応手順

A mixture of 4-(2-chlorophenyl)-2-(2-hydroxyimino-ethoxymethyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylic acid 3-ethyl 5-methyl ester (IBa, 150 mg), palladium hydroxide on carbon (10 mg) and ammonium formate (224 mg) in methanol (10 mL) was refluxed for 5 h under a nitrogen atmosphere. On cooling to room temperature, the mixture was filtered through a pad of celite. The filtrate was concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (grade 9385, Merck, 230-400 mesh, 60 Å) using a solvent mixture of dichloromethane and methanol (9:1; 100 mL), and dichloromethane, methanol and ammonium hydroxide (90:10:1; 500 mL) as eluent afforded the title compound (IAa 88 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723618
出典データセットuspto-grants-1998_03
ORD IDord-db51435d97f64dfb86f4de59e3efb185
出典メモuspto-grants-1998_03