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HRID 1845168作成日:2026年10月25日

Diisopropylethylamine → (R)-N3-(3-Hydroxy-1-(6-methylpyridin-3-yl)propyl)-N5-isobutyl-N5,4'-dimethylbiphenyl-3,5-dicarboxamide

https://huagongshe.com/reaction/1845168

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物(R)-3-Amino-3-(6-methylpyridin-3-yl)propan-1-olHCID 58103597—
反応物5-(Isobutyl(methyl)carbamoyl)-4'-methylbiphenyl-3-carboxylic acidHCID 58188089—
溶媒DichloromethaneHCID 6344—
生成物(R)-N3-(3-Hydroxy-1-(6-methylpyridin-3-yl)propyl)-N5-isobutyl-N5,4'-dimethylbiphenyl-3,5-dicarboxamideHCID 58187943—

反応手順

To a mixture of 5-(isobutyl(methyl)carbamoyl)-4′-methylbiphenyl-3-carboxylic acid (15 mg, 0.046 mmol), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (18 mg, 0.092 mmol), 1-hydroxybenzotriazole hydrate (7.0 mg, 0.046 mmol), and CH2Cl2 (2 mL) were added (R)-3-amino-3-(6-methylpyridin-3-yl)propan-1-ol (11 mg, 0.069 mmol) (WO 2008/130481) and N,N-diisopropylethylamine (12 μL, 0.069 mmol). The mixture was stirred at room temperature overnight, and then concentrated in vacuo. The residue was purified by preparative HPLC (100×21.2 mm C18 column, 40-70% MeCN/water[10 mM Et2NH]) to afford a white foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08946439B2
出典データセットuspto-grants-2015_02
ORD IDord-1b2dcdc35cb943499c4eee88f8fce025
出典メモuspto-grants-2015_02