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HRID 1806353作成日:2026年10月25日

2-Methylbutylamine, (S)- → [5-({[(2S)-2-methylbutyl]amino}methyl)-2-thienyl]boronic acid

https://huagongshe.com/reaction/1806353

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methylbutylamine, (S)-HCID 2724272—
反応物5-Formyl-2-thiopheneboronic acidHCID 2773430—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(5-{[(2-methylbutyl)amino]methyl}-2-thienyl)-1H-indole-7-carboxamideHCID 57732791—
生成物[5-({[(2S)-2-methylbutyl]amino}methyl)-2-thienyl]boronic acidHCID 66723247—

反応手順

Following the general procedure of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(5-{[(2-methylbutyl)amino]methyl}-2-thienyl)-1H-indole-7-carboxamide, (5-formyl-2-thienyl)boronic acid (50 mg, 0.32 mmol), [(2S)-2-methylbutyl]amine (28 mg, 0.32 mmol), and NaCNBH3 (40 mg, 0.64 mmol) were reacted to give 43 mg of crude [5-({[(2S)-2-methylbutyl]amino}methyl)-2-thienyl]boronic acid. The crude [5-({[(2S)-2-methylbutyl]amino}methyl)-2-thienyl]boronic acid was then reacted with 5-bromo-3-[1-(ethylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamide (65 mg, 0.157 mmol), K2CO3 (130 mg, 0.942 mmol), and tetrakis(triphenylphosphine)palladium(0) (4 mg, 0.003 mmol) to give 37.6 mg of the title compound (39%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08354406B2
出典データセットuspto-grants-2013_01
ORD IDord-07dfe055f3394430a3afd6078d3ba103
出典メモuspto-grants-2013_01