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HRID 545403作成日:2026年10月24日

((R)-1-Piperidin-4-yl-pyrrolidin-2-yl)-methanol di-hydrochloride → [2-(3-Hexyl-phenyl)-5-iodo-3-methyl-3H-imidazol-4-yl]-[4-((R)-2-hydroxymethyl-pyrrolidin-1-yl)-piperidin-1-yl]-methanone

https://huagongshe.com/ja/reaction/545403

反応式

関与物質

役割名称HCID仕込み量
反応物((R)-1-Piperidin-4-yl-pyrrolidin-2-yl)-methanol di-hydrochlorideHCID 67133026—
反応物2-(3-Hexyl-phenyl)-5-iodo-3-methyl-3H-imidazole-4-carboxylic acidHCID 67133239—
生成物[2-(3-Hexyl-phenyl)-5-iodo-3-methyl-3H-imidazol-4-yl]-[4-((R)-2-hydroxymethyl-pyrrolidin-1-yl)-piperidin-1-yl]-methanoneHCID 57541141—

反応手順

In analogy to the procedure described for example 2, 2-(3-hexyl-phenyl)-5-iodo-3-methyl-3H-imidazole-4-carboxylic acid (intermediate 1) and ((R)-1-piperidin-4-yl-pyrrolidin-2-yl)-methanol di-hydrochloride (intermediate 2) gave the title compound as light red amorphous solid. MS: 579.3 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07935707B2
出典データセットuspto-grants-2011_05
ORD IDord-8644913ba96e4da29633a33912dcbc58
出典メモuspto-grants-2011_05