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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58853생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물5-BromoindoleHCID 24905—
반응물(R)-2-Benzyloxycarbonylamino-3-iodo-propionic acid methyl esterHCID 10915437—
촉매ZincHCID 23994—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물(S)-methyl 2-(benzyloxycarbonylamino)-3-(1H-indol-5-yl)propanoateHCID 11760807371.4%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434761B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-7ddbbc0e8fed4be386b1454272ad4211
출처 메모uspto-grants-2016_09