戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 427299作成日:2026年10月25日

Oxalyl chloride → 2-Ethyl-4-methoxybenzothiazole-7-carboxylic acid (4-cyano-2-methyl-2H-pyrazol-3-yl)amide

https://huagongshe.com/reaction/427299

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物5-Amino-1-methyl-1H-pyrazole-4-carbonitrileHCID 219740—
反応物2-Ethyl-4-methoxybenzothiazole-7-carboxylic acidHCID 18357000—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物2-Ethyl-4-methoxybenzothiazole-7-carboxylic acid (4-cyano-2-methyl-2H-pyrazol-3-yl)amideHCID 990256661.2%

反応手順

To a suspension of 2-ethyl-4-methoxybenzothiazole-7-carboxylic acid (0.1 g) in dichloromethane (10 ml) was added oxalyl chloride (1.0 ml) and dimethylformamide (1 drop). The reaction was stirred at room temperature for 16 hrs, and then the solvent was removed in vacuo to yield a brown solid residue. 5-Amino-1-methyl-1H-pyrazole-4-carbonitrile (0.1 g) was taken up in dichloromethane (10 ml) and sodium hexamethyldisilylamine (1.0M in tetrahydrofuran, 0.84 ml) was added. After 5 minutes the acid chloride was added and the reaction stirred at room temperature for 16 hrs. The solvent was removed in vacuo and the product purified by flash chromatography (eluent 50% ethyl acetatethexane-75% ethyl acetate/hexane) to yield the title compound as an off-white solid (0.088 g). TLC Rf 0.13 (50% ethyl acetate/hexane); Mpt 190-191° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313116B1
出典データセットuspto-grants-2001_11
ORD IDord-804bd101a72849ae89ecd9eda9936a54
出典メモuspto-grants-2001_11