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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 427299Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt5-Amino-1-methyl-1H-pyrazole-4-carbonitrileHCID 219740—
Edukt2-Ethyl-4-methoxybenzothiazole-7-carboxylic acidHCID 18357000—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Ethyl-4-methoxybenzothiazole-7-carboxylic acid (4-cyano-2-methyl-2H-pyrazol-3-yl)amideHCID 990256661,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06313116B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-804bd101a72849ae89ecd9eda9936a54
Quellennotizuspto-grants-2001_11