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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 427299생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/427299

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물5-Amino-1-methyl-1H-pyrazole-4-carbonitrileHCID 219740—
반응물2-Ethyl-4-methoxybenzothiazole-7-carboxylic acidHCID 18357000—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-Ethyl-4-methoxybenzothiazole-7-carboxylic acid (4-cyano-2-methyl-2H-pyrazol-3-yl)amideHCID 990256661.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313116B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-804bd101a72849ae89ecd9eda9936a54
출처 메모uspto-grants-2001_11