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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 883952생성일: 2026년 10월 26일

Sodium Acetate → 5-[4-(4-Bromo-phenylcarbamoyl)-2-nitro-phenylsulfanyl]-indole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/883952

반응식

참여 물질

역할이름HCID투입량
반응물Sodium AcetateHCID 517045—
반응물N-(4-bromophenyl)-4-chloro-3-nitrobenzamideHCID 1068537—
반응물5-Mercapto-indole-1-carboxylic acid tert-butyl esterHCID 67040248—
용매EthanolHCID 702—
생성물5-[4-(4-Bromo-phenylcarbamoyl)-2-nitro-phenylsulfanyl]-indole-1-carboxylic acid tert-butyl esterHCID 6704099685%

반응 단계

A solution of the product of Example 59C (39.9 mg, 0.160 mmol) in anhydrous ethanol (2 mL) under a nitrogen atmosphere was treated with the product of Example 49A (56.8 mg, 0.160 mmol) and anhydrous sodium acetate (66 mg, 0.800 mmol) at room temperature, then heated at reflux for 2 hours. The reaction was cooled to room temperature and the solvent removed by rotary evaporation under vacuum. The residue was taken up in ethyl acetate (50 mL) and washed with water (2×25 mL) and brine (25 mL). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. Purification by silica gel flash chromatography using methylene chloride as eluent afforded the title compound as a yellow solid (77 mg, 85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08236950B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-d69c1fb25acb42a79c1b358340983ce4
출처 메모uspto-grants-2012_08