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HRID 1372790作成日:2026年10月27日

Triethylamine → HCID 44607520、化合物

https://huagongshe.com/reaction/1372790

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物Ethyl 4-amino-5-chloro-2-fluorophenylacetateHCID 17858807—
反応物1-((4-methoxyphenyl)methyl)-1H-indazole-3-carboxylic acidHCID 17859444—
触媒DimethylformamideHCID 6228—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物HCID 44607520HCID 4460752080%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07157487B2
出典データセットuspto-grants-2007_01
ORD IDord-64b3635a170d46b38d678f7ccc43fbfc
出典メモuspto-grants-2007_01