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HRID 1275443作成日:2026年10月26日

Triethylamine → 8-Chloro-6-(1-ethylpyrazol-5-yl)oxycarbonyl-5-methylthiochroman-4-one

https://huagongshe.com/reaction/1275443

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Thionyl ChlorideHCID 24386—
反応物6-Carboxy-8-chloro-5-methylthiochroman-4-oneHCID 22118434—
反応物HCID 178418331HCID 178418331—
溶媒DichloromethaneHCID 6344—
生成物8-Chloro-6-(1-ethylpyrazol-5-yl)oxycarbonyl-5-methylthiochroman-4-oneHCID 2211844784%

反応条件

温度40 °C

反応手順

A mixture containing 2.0 g (7.8 mmol) of 6-carboxy-8-chloro-5-methylthiochroman-4-one and 2.8 g (3.0 eq., 24 mmol) of thionyl chloride was stirred under heat at 40° C. for 2 hours. After the completion of the reaction, excess thionyl chloride was removed under reduced pressure. Then, the resultant acid chloride was dissolved in 10 ml of methylene chloride, and 0.96 g (1.1 eq., 8.6 mmol) of 1-ethyl-5-hydroxypyrazole and 0.95 ml (9.41 mmol) of triethylamine were added. The mixture was stirred at room temperature for 3 hours. The reaction mixture was diluted with methylene chloride, washed with diluted hydrochloric acid and with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate, and the solvent was distilled off to give 2.29 g (yield 84%) of 8-chloro-6-(1-ethylpyrazol-5-yl)oxycarbonyl-5-methylthiochroman-4-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06159904
出典データセットuspto-grants-2000_12
ORD IDord-9215bac86bf34079ba382215c1c3bc05
出典メモuspto-grants-2000_12