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HRID 32056作成日:2026年10月24日

Isopropylamine → N-[7-(isopropylamino-methyl)-chroman-4-yl]-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide

https://huagongshe.com/ja/reaction/32056

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropylamineHCID 6363—
反応物DiisopropylethylamineHCID 81531—
反応物Methanesulfonic anhydrideHCID 81560—
反応物N-(7-hydroxymethyl-chroman-4-yl)-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamideHCID 68932544—
溶媒ChloroformHCID 6212—
溶媒TetrahydrofuranHCID 8028—
生成物N-[7-(isopropylamino-methyl)-chroman-4-yl]-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamideHCID 68928313—

反応条件

温度0 °C

反応手順

N-(7-Hydroxymethyl-chroman-4-yl)-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide (Step A) (0.050 g, 0.010 mmol) and DIEA (0.038 g, 0.030 mmol) were dissolved in THF (1.5 mL). The solution was cooled to 0° C. and methanesulfonic anhydride (0.023 g, 0.014 mmol) was added. After the reaction was stirred for 3.5 h, isopropylamine (0.14 g, 2.3 mmol) was added and the solution was stirred at RT overnight. The reaction was diluted with CHCl3 and washed with brine. The aqueous phase was extracted once with CHCl3. The organic phases were combined, dried over MgSO4, filtered, and concentrated in vacuo to provide a residue which was purified by column chromatography (silica, 0.2% TEA in acetone) to provide the title compound. MS (ESI) m/z 558 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425631B2
出典データセットuspto-grants-2008_09
ORD IDord-5e3421b9ffec4c83ab2a6feeab9ea2e4
出典メモuspto-grants-2008_09