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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1372790생성일: 2026년 10월 26일

Triethylamine → HCID 44607520, 화합물

https://huagongshe.com/reaction/1372790

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물Ethyl 4-amino-5-chloro-2-fluorophenylacetateHCID 17858807—
반응물1-((4-methoxyphenyl)methyl)-1H-indazole-3-carboxylic acidHCID 17859444—
촉매DimethylformamideHCID 6228—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물HCID 44607520HCID 4460752080%

반응 단계

In methylene chloride (10 ml) was dissolved 1-(4-methoxybenzyl)-3-indazolylcarboxylic acid (630 mg, 2.23 mmol). To the resulting solution were added oxalyl chloride (292 μl, 3.53 mmol) and DMF (1 drop). The resulting mixture was stirred until the mixture became uniform. From the reaction mixture, the solvent was distilled off under reduced pressure. The residue was dissolved in methylene chloride (20 ml). Ethyl (4-amino-5-chloro-2-fluorophenyl)acetate (517 mg, 2.23 mmol) and triethylamine (621 μl, 4.46 mmol) were added to the resulting solution. The resulting mixture was heated under reflux for 15 hours. After cooling, the reaction mixture was added with water (50 ml), followed by extraction with chloroform (200 ml). The extract was dried over anhydrous magnesium 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 (4:1) eluate fractions, ethyl (5-chloro-2-fluoro-4-(1-(4-methoxybenzyl)-3-indazolylcarbonylamino)phenyl)acetate (881 mg, 80%) was obtained as a pale yellow amorphous substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07157487B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-64b3635a170d46b38d678f7ccc43fbfc
출처 메모uspto-grants-2007_01