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HRID 58853作成日:2026年10月24日

Iodine → (S)-methyl 2-(benzyloxycarbonylamino)-3-(1H-indol-5-yl)propanoate

https://huagongshe.com/ja/reaction/58853

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物5-BromoindoleHCID 24905—
反応物(R)-2-Benzyloxycarbonylamino-3-iodo-propionic acid methyl esterHCID 10915437—
触媒ZincHCID 23994—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
触媒2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物(S)-methyl 2-(benzyloxycarbonylamino)-3-(1H-indol-5-yl)propanoateHCID 11760807371.4%

反応手順

To a suspension of zinc (2.53 g, 38.8 mmol) in DMF (20 mL) was added I2 (1.10 g, 4.15 mol) followed by addition of a solution of (R)-methyl 2-(benzyloxycarbonylamino)-3-iodopropanoate (4.70 g, 13.0 mmol) in DMF (20 mL). The mixture was stirred at ambient temperature for 5 min and heated at 35° C. for 40 min. Then a solution of 5-bromo-1H-indole (3.00 g, 15.5 mmol) in DMF (10 mL), Pd2(dba)3 (0.25 g, 0.27 mmol) and S—Phos (0.25 g, 0.60 mmol) were added. The reaction mixture was stirred at 50° C. under nitrogen overnight and then cooled to ambient temperature. Brine (500 mL) was added and the resulting mixture was extracted with EtOAc (200 mL×3). The organics were combined, washed with brine (300 mL) and concentrated. The residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=10:1 to 5:1) to afford (S)-methyl 2-(benzyloxycarbonylamino)-3-(1H-indol-5-yl)propanoate as a viscous oil (3.27 g, 60% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434761B2
出典データセットuspto-grants-2016_09
ORD IDord-7ddbbc0e8fed4be386b1454272ad4211
出典メモuspto-grants-2016_09