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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1372707생성일: 2026년 10월 26일

Triethylamine → Ethyl (5-chloro-2-fluoro-4-(((5-fluoro-1-methyl-3-indolyl)carbonyl)amino)phenyl)acetate

https://huagongshe.com/reaction/1372707

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물Ethyl 4-amino-5-chloro-2-fluorophenylacetateHCID 17858807—
반응물5-fluoro-1-methyl-1H-indole-3-carboxylic acidHCID 18385102—
용매Hydrochloric AcidHCID 313—
용매DichloromethaneHCID 6344—
생성물Ethyl (5-chloro-2-fluoro-4-(((5-fluoro-1-methyl-3-indolyl)carbonyl)amino)phenyl)acetateHCID 5877839747%

반응 조건

온도0 °C

반응 단계

In methylene chloride (30 ml) was dissolved 5-fluoro-1-methylindole-3-carboxylic acid (885 mg, 4.58 mmol). To the resulting solution was added oxalyl chloride (600 μl, 6.87 mmol) under stirring at 0° C., and the resulting mixture was stirred at room temperature for 1 hour. From the reaction mixture, the solvent was distilled off under reduced pressure. The residue was dissolved in methylene chloride (50 ml). The resulting solution was added dropwise to a solution of ethyl (4-amino-5-chloro-2-fluorophenyl)acetate (1.06 g, 4.58 mmol) in methylene chloride (20 ml), followed by heating under reflux for 15 minutes. The reaction mixture was cooled and triethylamine (3.19 ml, 22.9 mmol) was added thereto. The resulting mixture was heated under reflux for 18 hours. The reaction mixture was cooled and poured in 1N HCl, followed by extraction with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from hexane/ethyl acetate (2/1) eluate fractions, ethyl (5-chloro-2-fluoro-4-(((5-fluoro-1-methyl-3-indolyl)carbonyl)amino)phenyl)acetate (868 mg, 47%) was obtained as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07157487B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-9a7ef896ad7749caa06334d43bd175d7
출처 메모uspto-grants-2007_01