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HRID 632576作成日:2026年10月24日

Sodium Bicarbonate → 1-cyclopentyl N-{3-[(methylamino)methyl]benzyl}-L-leucinate

https://huagongshe.com/ja/reaction/632576

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物Methylamine hydrochlorideHCID 6364545—
反応物3-(Bromomethyl)benzaldehydeHCID 7127825—
反応物L-leucine cyclopentyl ester tosylateHCID 86633653—
溶媒MethanolHCID 887—
溶媒1,1-DichloroethaneHCID 6365—
溶媒Ethyl AcetateHCID 8857—
生成物1-cyclopentyl N-{3-[(methylamino)methyl]benzyl}-L-leucinateHCID 8668642615.2%

反応手順

To a solution of 3-(bromomethyl)-benzaldehyde (0.513 g, 2.57 mmol) in dichloroethane (10 mL) was added L-leucine cyclopentyl ester tosylate (1.29 g, 3.46 mmol) and sodium triacetoxyborohydride (1.37 g, 6.46 mmol). The mixture was stirred for 30 minutes at room temperature then poured into ethyl acetate (200 mL). The organic extracts were washed with saturated ammonium chloride (2 times 50 mL) and water (50 mL). The organic extracts were then dried (MgSO4) and concentrated. The residue was dissolved in ethanol (30 mL) and methylamine hydrochloride (4.17 g, 61.7 mmol) was added followed by sodium hydrogen carbonate (4.32 g, 51 mmol). The mixture was stirred at room temperature for 18 hours then concentrated under vacuum, loaded directly onto a silica gel column and eluted with 95:5 dichloromethane:methanol to yield the desired product (0.130 g, 15% yield). LC/MS: m/z 333.25 [M+H]+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09321718B2
出典データセットuspto-grants-2016_04
ORD IDord-91e262448bd24c2a981e1bc01796de64
出典メモuspto-grants-2016_04